Multi-event September 2018 FDA Recall Drug by Right Value Drug Stores, Inc.

This Multi-event Class III drug recall was voluntarily initiated by Right Value Drug Stores, Inc. on September 25, 2018 for the product Drug. The FDA reported the reason for recall as labeling not elsewhere classified. The product was distributed in Distributed in California and the recall is currently terminated.

Reported Recall Events

D-0242-2019 TERMINATED D-0241-2019 TERMINATED D-0240-2019 TERMINATED D-0243-2019 TERMINATED

Recall Number: D-0242-2019

Reason for Recall
Labeling Not Elsewhere Classified: Misbranding.
Initiated
09-25-2018
Reported
11-21-2018
Quantity
660 capsules

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
81198
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Right Value Drug Stores, 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.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Distributed in California
Termination Date About Termination Date
Date that FDA officially terminated the recall.
10-13-2020
Product Description About Product Description
Full technical description of the product.
Tadalafil SR 7 mg Capsules packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054. NDC 99999-9970-88

Batch or Lot Expiration Information

Lot# Lots: 04242018@16 Exp. 10/21/2018; 05042018@17 Exp. 10/31/2018; 07232018@13 Exp. 01/19/2019; 08032018@2 Exp. 01/30/2019

Recall Number: D-0241-2019

Reason for Recall
Labeling Not Elsewhere Classified: Misbranding.
Initiated
09-25-2018
Reported
11-21-2018
Quantity
8240 capsules

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
81198
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Right Value Drug Stores, 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.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Distributed in California
Termination Date About Termination Date
Date that FDA officially terminated the recall.
10-13-2020
Product Description About Product Description
Full technical description of the product.
Progesterone SR 200 mg Capsules, packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376. NDC 99999-0018-74

Batch or Lot Expiration Information

Lot# Lots: 04052018@16 Exp. 9/11/2018; 04242018@2 Exp. 10/21/2018; 05072018@8 Exp. 10/21/2018; 05302018@3 Exp. 10/22/2018; 06192018@9 Exp. 10/22/2018; 06192018@10 Exp. 12/15/2018; 06202018@12 Exp. 12/15/2018; 07022018@15 Exp. 12/15/2018; 07242018@2 Exp. 1/13/2018; 08312018@3 Exp. 2/6/2018

Recall Number: D-0240-2019

Reason for Recall
Labeling Not Elsewhere Classified: Misbranding.
Initiated
09-25-2018
Reported
11-21-2018
Quantity
6580 capsules

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
81198
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Right Value Drug Stores, 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.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Distributed in California
Termination Date About Termination Date
Date that FDA officially terminated the recall.
10-13-2020
Product Description About Product Description
Full technical description of the product.
Progesterone SR 100 mg Capsules, packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376. NDC 99999-0104-55

Batch or Lot Expiration Information

Lot# Lots: 03272018@10 Exp. 09/11/2018; 03282018@8 Exp. 09/24/2018; 03282018@18 Exp. 09/24/2018; 04232018@3 Exp. 09/24/2018; 05302018@4 Exp. 10/22/2018; 06072018@6 Exp. 10/22/2018; 06212018@1 Exp. 10/22/2018; 06252018@7 Exp. 10/22/2018; 07192018@8 Exp. 10/22/2018; 07192018@10 Exp. 01/15/2019; 08282018@6 Exp. 2/23/2019; 08282018@7 Exp. 2/23/2019; 09142018@1 Exp. 02/23/2018; 09182018@10 Exp. 2/23/2019

Recall Number: D-0243-2019

Reason for Recall
Labeling Not Elsewhere Classified: Misbranding.
Initiated
09-25-2018
Reported
11-21-2018
Quantity
180 capsules

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
81198
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class III - is a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Right Value Drug Stores, 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.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Distributed in California
Termination Date About Termination Date
Date that FDA officially terminated the recall.
10-13-2020
Product Description About Product Description
Full technical description of the product.
Tadalafil SR 12 mg Capsules packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop 122 Grapevine Hwy. Hurst, TX 76054 817-282-9376 NDC 99999-9969-51

Batch or Lot Expiration Information

Lot# Lots: 07232018@15 Exp. 1/19/2019; 08102018@10 Exp. 2/6/2019