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Class II · ModerateActive recall

Lacosamide

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot: A253999, A254000, Expires: 09/30/2027.
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byCamber Pharmaceuticals, Inc.
Brand nameLACOSAMIDE
Generic nameLACOSAMIDE
Active ingredient(s)LACOSAMIDE
Distributed by / forCamber Pharmaceuticals, Inc., Piscataway, NJ 08854
NDC31722-813-60
Show the full FDA record
Full product labelLacosamide 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.
Recalling firmAnnora Pharma Private Limited
DistributionNationwide in the USA
Quantity31,392 60-count bottles
Recall initiated2026-06-04
Report date2026-07-01
Recall completed—
Recall numberD-0626-2026
ClassificationClass II
FDA statusOngoing
Origin on fileHyderabad N/A India

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.