Data Foundry

Drug recalls 2026

Perampanel CIII Tablets — Class II drug recall D-0628-2026

Ongoing recall by SUN PHARMACEUTICAL INDUSTRIES INC, reported 2026-07-01, distributed nationwide. Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6

Recall numberD-0628-2026
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSUN PHARMACEUTICAL INDUSTRIES INC, Princeton, NJ, United States
Recall initiated2026-06-17
Classified2026-06-26
Reported by FDA2026-07-01
DistributedNationwide (US)
Reason classeslabeling
NDC51672-4204, 51672-4204-03, 51672-4204-06, 51672-4205, 51672-4205-02, 51672-4205-06, 51672-4206, 51672-4206-02, 51672-4206-06, 51672-4207, 51672-4207-02, 51672-4207-06, 51672-4208, 51672-4208-02, 51672-4208-06, 51672-4209, 51672-4209-02, 51672-4209-06
Lot numbersAE01763
Expiration dates2027-09-30

Product

Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 51672-4206-6

Reason for recall

Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.

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-0628-2026. 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.