US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 19, 2025 (15 months ago)

Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective container; blister packaging inadequately sealed.

What was recalled

Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, NDC 0904-6665-61

Recalling firm
The Harvard Drug Group LLC
NDC code
0904-6665-61
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0507-2025

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.

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