FDA-Drug2026-07-01Class IIPACKAGING DEFECT
Camber Pharmaceuticals Lacosamide 100mg tablets recalled for wrong drug in bottle
TAMPERINGNationwide distribution
Camber Lacosamide tablets recalled for Selexipag mix-up
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.
Hazard
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
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-0626-2026Don't want to check this manually?
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