Data Foundry

Drug recalls 2026

Lacosamide Tablets — Class II drug recall D-0626-2026

Ongoing recall by Annora Pharma Private Limited, reported 2026-07-01, distributed nationwide. Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of

Recall numberD-0626-2026
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAnnora Pharma Private Limited, Hyderabad, N/A, India
Recall initiated2026-06-04
Classified2026-06-25
Reported by FDA2026-07-01
DistributedNationwide (US)
NDC31722-0812, 31722-0812-05, 31722-0812-18, 31722-0812-32, 31722-0812-60, 31722-0813, 31722-0813-05, 31722-0813-18, 31722-0813-32, 31722-0813-60, 31722-0814, 31722-0814-05, 31722-0814-18, 31722-0814-32, 31722-0814-60, 31722-0815, 31722-0815-05, 31722-0815-18, 31722-0815-32, 31722-0815-60
Lot numbersA253999, A254000
Expiration dates2027-09-30

Product

Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313, Telangana, India, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, NDC 31722-813-60.

Reason for recall

Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.

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-0626-2026. 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.