D-1527-2016 Class III Terminated
FDA drug recall D-1527-2016 was initiated by Mckesson Packaging Services on September 15, 2016 and is designated Class III. 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). The recall status is terminated (terminated May 3, 2017). Affected quantity: 3,492 unit cartons of 10 x 10 blister cards.
Recall Details
- Product Type
- Drugs
- Report Date
- October 5, 2016
- Initiation Date
- September 15, 2016
- Termination Date
- May 3, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3,492 unit cartons of 10 x 10 blister cards
Product Description
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
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).
Distribution Pattern
CO, IL, LA, OH
Code Information
Lot #: 0111512; Exp. 08/17