RecallRadar

FDA Drug recall D-0508-2025

Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN…

On 2025-07-09 the FDA classified a Class II recall of Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN… by The Harvard Drug Group, citing defective container; blister packaging inadequately sealed.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0508-2025
ClassificationClass II
Statusongoing
Initiated2025-06-19
Published2025-07-09
Last updated2026-09-13 11:52 UTC
CompanyThe Harvard Drug Group
DistributionUS

Product

Gabapentin Capsules, USP, 100 mg, 10 capsules (10x1) per bag, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN, 46268 USA, Distributed by Cardinal Health, Dublin, OH 43017, NDC 55154-3363-0

Reason

Defective container; blister packaging inadequately sealed.

Identifiers

ndc55154-3363-0
ndc55154-7992-0
ndc55154-7993-0
code_infoLot# M05205A and M05205B, Exp Date 10/2026.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0508-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.