Multi-event June 2015 FDA Recall Drug by Life Science Pharmacy Inc

This Multi-event Class II drug recall was voluntarily initiated by Life Science Pharmacy Inc on June 8, 2015 for the product Drug. The FDA reported the reason for recall as penicillin cross contamination. The product was distributed Nationwide and the recall is currently terminated.

Reported Recall Events

D-0501-2016 TERMINATED D-0491-2016 TERMINATED D-0496-2016 TERMINATED D-0497-2016 TERMINATED D-0490-2016 TERMINATED D-0494-2016 TERMINATED D-0489-2016 TERMINATED D-0492-2016 TERMINATED D-0486-2016 TERMINATED D-0493-2016 TERMINATED D-0499-2016 TERMINATED D-0503-2016 TERMINATED D-0504-2016 TERMINATED D-0502-2016 TERMINATED D-0487-2016 TERMINATED D-0500-2016 TERMINATED D-0507-2016 TERMINATED D-0508-2016 TERMINATED D-0498-2016 TERMINATED D-0488-2016 TERMINATED D-0495-2016 TERMINATED D-0506-2016 TERMINATED D-0505-2016 TERMINATED

Recall Number: D-0501-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
TRI-EST Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0491-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Suppositories, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0496-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
BI-EST Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0497-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
BI-EST Gels, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0490-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Vaginal Creams, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0494-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Creams, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0489-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0492-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Vaginal Gels, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0486-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
2-DEOXY-D-GLUCOSE Powder, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# all lots

Recall Number: D-0493-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Face Creams, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0499-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
BI-EST Suspensions, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0503-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
TRI-EST Liquids, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0504-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
TRI-EST Gels, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0502-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
TRI-EST Lozenges, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0487-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
E3 CREAM, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# Lot: 02-11-15 14:44 Y, Exp Date: 08/10/15

Recall Number: D-0500-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
BI-EST Creams, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0507-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
HUMAN CHORIONIC GONADOTROPIC (HCG) Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0508-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
HUMAN CHORIONIC GONADOTROPIC (HCG) Sublingual Drops, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0498-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
BI-EST Lozenges, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0488-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
HYDROXOCOBALAMIN Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# all lot numbers, all expiration dates

Recall Number: D-0495-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
ESTRIOL Gels, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0506-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
METHYLFOLATE Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots

Recall Number: D-0505-2016

Reason for Recall
Penicillin Cross Contamination: potentially contaminated with penicillin
Initiated
06-08-2015
Reported
12-09-2015
Quantity
unknown

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71494
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Life Science Pharmacy Inc
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Telephone
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
06-11-2018
Product Description About Product Description
Full technical description of the product.
METHYLFOLATE Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

Batch or Lot Expiration Information

Lot# All lots