D-1449-2014 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- July 30, 2014
- Initiation Date
- September 27, 2011
- Termination Date
- July 31, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 99/500 mg tablets
Product Description
Pramipexole Dihydrochloride Tablets, 0.5 mg, Rx, packaged and labeled to contain Nebivolol tablets, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Northstar Rx, Memphis, TN NDC 16714-586-01
Reason for Recall
Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets
Distribution Pattern
Product was shipped to the following states: CO, MA, OH, TX & WY.
Code Information
Use by 12/14/2012, Lot# 002B90, NDC 16714-586-01