US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 24, 2023 (3 years ago)

Gabapentin Tablets, USP 600 mg, packaged in Cartons of 100 tablets (10 tablets per…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Product mixup: one foreign tablet found in product.

What was recalled

Gabapentin Tablets, USP 600 mg, packaged in Cartons of 100 tablets (10 tablets per blister pack x 10), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. East Windsor, NJ 08520 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA, NDC 0904-6823-61

Recalling firm
The Harvard Drug Group
NDC code
0904-6823-61
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0570-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other East recalls

See all