SomerSET Therapeutics recalls Haloperidol decanoate injection 50mg/mL vials due to potential trace water contamination. This may cause adverse reactions. Check your vial lot numbers for affected batches.
Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
SomerSET Therapeutics is recalling Haloperidol decanoate injections that may contain trace amounts of water for injection. This could lead to adverse reactions if used improperly. Affected vials have specific lot numbers and expiration dates.
The injection may contain trace amounts of water for injection (WFI) which could cause adverse reactions when administered. This is a potential contamination risk during manufacturing in India.
Prescription patients using the recalled Haloperidol injections are affected. Healthcare providers handling these vials are at higher risk due to the medication's critical use.
Check for vials labeled 'Haloperidol decanoate Injection 50mg/mL' with lot numbers A230412A (expiring 07/2025) or A230412B (expiring 07/2025).
Identify affected vials by lot numbers A230412A or A230412B with expiration dates of 07/2025.
The recall states the product may contain trace water for injection, which could cause adverse reactions. Use only the unaffected vials.
Check your vial lot numbers. If they match A230412A or A230412B with expiration 07/2025, contact your healthcare provider for guidance.
Look for the lot numbers A230412A or A230412B on the vial with expiration date 07/2025.
We’ve drafted a message you can send SomerSET Therapeutics to request your refund or repair — edit it as you like.
Subject: Recall D-0506-2024 — SomerSET Therapeutics SomerSET Therapeutics Hello, I own a SomerSET Therapeutics that is covered by recall D-0506-2024 from SomerSET Therapeutics. 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.
