FDA recall record

Gabapentin Tablets USP, 600 mg recall — FDA D-1272-2020

Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.

Class IIIclassification
D-1272-2020official record ID
May 27, 2020report date

Recall record at a glance

Official recordD-1272-2020
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmInvaGen Pharmaceuticals, Inc.
Report dateMay 27, 2020
Recall initiation dateMay 14, 2020
Quantity2,202 bottles
LocationHauppauge, NY, United States

Official product description

Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc., Lawrenceville, GA 30046, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY 11788, NDC 76282-405-05.

Why the product was recalled

Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.

Distribution information

Nationwide in the U.S.

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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