D-1431-2019 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- July 3, 2019
- Initiation Date
- May 13, 2019
- Termination Date
- September 30, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3,015 cartons
Product Description
Pramipexole Dihydrochloride Tablets, 0.125 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-793-95; NDC Carton: 68084-793-25
Reason for Recall
GMP Deviations; possible cross contamination of product due to cleaning procedure failure.
Distribution Pattern
Nationwide USA
Code Information
Lot, expiry: Lot 179049, exp 12/31/2019; Lot 182571, exp 8/31/2020