D-1449-2014 Class II Terminated

Recalled by Shamrock Medical Solutions Group LLC — Lewis Center, OH

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