Reported Jul 30, 2014 · Terminated
Pramipexole Dihydrochloride Tablets, 0.5 mg, Rx, packaged and labeled to contain Nebivolol tablets, Repackaged By:…
Shamrock Medical Solutions Group LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Shamrock Medical Solutions Group LLC · 741 Radio Dr · Lewis Center, OH · 43035-7134
Is this the product you have?
- Pramipexole Dihydrochloride Tablets, 0.5 mg, Rx, packaged and labeled to contain Nebivolol tablets
- Repackaged ByShamrock Medical Solutions Lewis Center, Ohio
- MfgNorthstar Rx, Memphis, TN NDC 16714-586-01
- Lot codes and dates
Use by 12/14/2012Lot# 002B90NDC 16714-586-01
- Amount recalled
- 99/500 mg tablets
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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