Hikma recalls Infumorph morphine solution ampules due to expired filter in carton. This could lead to ineffective medication if used after expiration. Check your lot numbers for affected batches.
The filter included in the carton has an expiration date that has expired prior to the expiration date of the actual product lot.
Hikma is recalling Infumorph (preservative-free morphine sulfate) ampules because the filter in the carton expired before the product's expiration date. This means the filter might not work properly, potentially making the medication ineffective if used after the expiration date.
The filter in the carton has expired before the product's expiration date. This could mean the filter no longer functions properly, potentially leading to ineffective medication if the product is used after the expiration date.
Prescription patients using Infumorph morphine solution ampules with lot numbers 052001, 052003 (expiring 11/2024) or 023012, 023014 (expiring 08/2024) are affected. Healthcare providers and patients who use the product as directed are most at risk.
Check the lot numbers on the carton: 052001, 052003 (expiring 11/2024) or 023012, 023014 (expiring 08/2024). The product is a 20 mL ampule for prescription use only.
Look for lot numbers 052001, 052003 (expiring 11/2024) or 023012, 023014 (expiring 08/2024) on the carton.
The filter in the carton has expired before the product's expiration date, which could mean it no longer functions properly and might lead to ineffective medication.
The recall record does not specify a remedy, so no action is required beyond checking the lot numbers.
The product may be safe if used before the expiration date, but the expired filter could make it ineffective after that date.
We’ve drafted a message you can send Hikma to request your refund or repair — edit it as you like.
Subject: Recall D-0392-2024 — Hikma Hikma Hello, I own a Hikma that is covered by recall D-0392-2024 from Hikma. 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.
