FDAFDA · Food and drugs·Recall number D-1449-2014
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
Published July 30, 2014 · Recall initiated: September 27, 2011
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Shamrock Medical Solutions Group LLC
- Distributor
- Product was shipped to the following states: CO, MA, OH, TX & WY.
- Lot
- Use by 12/14/2012, Lot# 002B90, NDC 16714-586-01
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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