Lundbeck recalls Sabril oral solution (500mg, 50 packets) due to cross contamination with other products. Affected lots manufactured in Cincinnati, OH. No remedy specified in recall notice.
Cross contamination with other products
Lundbeck is recalling Sabril oral solution (500mg, 50 packets) because it may have been cross contaminated with other products. This could affect people taking this medication for seizures. The recall does not include a remedy.
Cross contamination with other products means the medication may contain harmful substances not intended for use. This could lead to adverse effects for people taking the medication, though the specific risks are not detailed in the recall notice.
People with a prescription for Sabril oral solution who received the recalled lots manufactured in Cincinnati, OH. Those most at risk are individuals taking this medication for seizure disorders.
Check the product label for Sabril (vigabatrin) oral solution, 500 mg, 50 packets. Look for lot numbers 3207333A, 3207334A (expiring 03/2027) or 3214707A, 3214709A, 3214710A (expiring 02/2028).
Look for the lot numbers 3207333A, 3207334A (expiring 03/2027) or 3214707A, 3214709A, 3214710A (expiring 02/2028) on the Sabril oral solution packaging.
The recall notice does not specify any remedy.
The product may have been cross contaminated with other products, which could lead to adverse effects for people taking the medication.
Lots 3207333A, 3207334A (expiring 03/2027) and 3214707A, 3214709A, 3214710A (expiring 02/2028).
We’ve drafted a message you can send Lundbeck to request your refund or repair — edit it as you like.
Subject: Recall D-1142-2023 — Lundbeck Lundbeck Hello, I own a Lundbeck that is covered by recall D-1142-2023 from Lundbeck. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
