July 2016 FDA Recall Drug by Medicap Pharmacy
D-1447-2016 - Lack of Assurance of Sterility

This Class II drug recall was voluntarily initiated by Medicap Pharmacy on July 7, 2016 for the product Drug. The FDA reported the reason for recall as lack of assurance of sterility. The product was distributed in ID and the recall is currently terminated.

Recall Number: D-1447-2016

Reason for Recall
Lack of Assurance of Sterility: Sterile products were not produced in a controlled, sterile environment.
Initiated
07-07-2016
Reported
08-03-2016
Quantity
1 bottle

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
74725
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.
Medicap Pharmacy
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.
ID
Termination Date About Termination Date
Date that FDA officially terminated the recall.
08-08-2016
Product Description About Product Description
Full technical description of the product.
Acetylcyst 10% OPHT SOL, 10%, 15 mL bottle, Rx only, Medicap Pharmacy, 2790 W Cherry Lane, Meridian, ID 83642, NDC 99999-9996-94.

Batch or Lot Expiration Information

Lot# : 05092016@19, Beyond Use Date: 06/08/16; Discard After 09/01/2017.