Data Foundry

Drug recalls 2025

Gabapentin Capsules — Class III drug recall D-0311-2025

Ongoing recall by SUN PHARMACEUTICAL INDUSTRIES INC, reported 2025-04-16, distributed nationwide. Cross Contamination

Recall numberD-0311-2025
Product typeDrug
ClassificationClass III
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSUN PHARMACEUTICAL INDUSTRIES INC, Princeton, NJ, United States
Recall initiated2025-03-04
Classified2025-04-04
Reported by FDA2025-04-16
DistributedNationwide (US)
Quantity12,876 bottles
NDC62756-0137, 62756-0137-01, 62756-0137-02, 62756-0137-03, 62756-0137-04, 62756-0137-05, 62756-0138, 62756-0138-01, 62756-0138-02, 62756-0138-03, 62756-0138-04, 62756-0138-05, 62756-0139, 62756-0139-01, 62756-0139-02, 62756-0139-03, 62756-0139-04, 62756-0139-05, 62756-0202, 62756-0202-01, 62756-0202-03, 62756-0204, 62756-0204-01, 62756-0204-03
Expiration dates2025-04, 2025-07, 2025-08

Product

Gabapentin Capsules, USP 300 mg, Rx Only, Packaged in a) 500-count bottles, NDC 62756-138-05; b) 1000-count bottles, NDC 62756-138-04, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway, Halol-389 350, Gujarat, India.

Reason for recall

Cross Contamination

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0311-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.