June 2015 FDA Recall Drug by American Health Packaging
D-1235-2015 - Tablets/Capsules Imprinted with Wrong ID

This Class III drug recall was voluntarily initiated by American Health Packaging on June 26, 2015 for the product Drug. The FDA reported the reason for recall as tablets/capsules imprinted with wrong id. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1235-2015

Reason for Recall
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
Initiated
06-26-2015
Reported
07-22-2015
Quantity
341 Cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
71634
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.
American Health Packaging
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.
U.S. Nationwide
Termination Date About Termination Date
Date that FDA officially terminated the recall.
08-15-2018
Product Description About Product Description
Full technical description of the product.
Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.

Batch or Lot Expiration Information

Lot# :151360, Expiry: 12/31/2016