September 2016 FDA Recall Drug by Mckesson Packaging Services
D-1527-2016 - Labeling

This Class III drug recall was voluntarily initiated by Mckesson Packaging Services on September 15, 2016 for the product Drug. The FDA reported the reason for recall as labeling. The product was distributed in CO, IL, LA, OH and the recall is currently terminated.

Recall Number: D-1527-2016

Reason for Recall
Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).
Initiated
09-15-2016
Reported
10-05-2016
Quantity
3,492 unit cartons of 10 x 10 blister cards

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
75215
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.
Mckesson Packaging Services
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.
CO, IL, LA, OH
Termination Date About Termination Date
Date that FDA officially terminated the recall.
05-03-2017
Product Description About Product Description
Full technical description of the product.
Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10

Batch or Lot Expiration Information

Lot# : 0111512; Exp. 08/17