FDA-Drug2026-07-01Class IIPACKAGING DEFECT
Camber Pharmaceuticals Lacosamide 100mg tablets recalled for wrong drug in bottle
What this means
Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.
- Check your bottle against lots A253999 or A254000 (expiration 09/30/2027).
- Do not take tablets from affected bottles.
- Contact your pharmacist or doctor to verify your medication and get a replacement if needed.
- Return the bottle to the pharmacy.
The agency's original wording
Hazard
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
Intended for
Adults
Illnesses reported
None reported
Sold states
Nationwide in the USA
Affected count
31,392 60-count bottles
Manufactured in
Sy. No.261, Plot No. 13 And 14, Annaram Village, Gummadidal Mandal, Jinnaram Mandal, Sangareddy District, Medak, Hyderabad, N/A, India
Products
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0626-2026Want us to check the next one for you?
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