D-1350-2015 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- August 26, 2015
- Initiation Date
- August 13, 2015
- Termination Date
- August 21, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 360 Bottles
Product Description
AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland Ltd., Clonmel, Ireland, NDC: 67253-180-50
Reason for Recall
Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.
Distribution Pattern
U.S. Including: OH
Code Information
Lot #: 52217, Expiry: 04/18