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Parkinson’s Med Recalled
06/23/2016
More than 12,500 bottles of pramipexole dihydrochloride extended-release tablets, 0.375 mg, are being recalled nationwide and in Puerto Rico.
What’s the reason for the Class III recall? Drug manufacturer Par Pharmaceutical reported that it launched the recall due to the presence of a known impurity that is above current specification levels.
The following lots are being recalled.
|
Lot |
Expiration |
|
27409201 |
February 2017 |
|
27409301 |
February 2017 |
|
27409401 |
February 2017 |
|
27662101 |
July 2017 |
Click here to read the report.
--Stephanie Vaccaro
Reference:
US Food and Drug Administration. FDA Enforcement Report – Week of June 22, 2016. www.fda.gov. Accessed June 23, 2016.
