FDA recall record

Sandoz Pramipexole Dihydrochloride Tablets, 0.125 mg, 90-count tablets per bottle recall — FDA D-1678-2012

Impurities/Degradation Products: An out of specification result for a known impurity of the product occurred during 12 month stability testing.

Class IIIclassification
D-1678-2012official record ID
Sep 26, 2012report date

Recall record at a glance

Official recordD-1678-2012
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmSandoz Inc.
Report dateSep 26, 2012
Recall initiation dateSep 12, 2012
Quantity41,761bottles.
LocationBroomfield, CO, United States

Official product description

Pramipexole Dihydrochloride Tablets, 0.125 mg, 90-count tablets per bottle, Rx only, Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Princeton, NJ 08540, NDC 0781-5248-92

Why the product was recalled

Impurities/Degradation Products: An out of specification result for a known impurity of the product occurred during 12 month stability testing.

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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