Nephron recalls morphine syringes due to potential contamination. Affected units have specific NDC and expiration dates. Consumers should contact Nephron for details.
Lack of Assurance of Sterility
Nephron is recalling morphine syringes that may not be sterile, which could lead to infections if used. This is a serious safety issue for patients receiving the medication.
The syringes were produced at a facility that may not have maintained proper sterility standards. If the syringes are not sterile, injecting them could cause infections or other health issues.
Patients using the recalled morphine syringes for pain management are at risk. Healthcare providers who have these syringes in their inventory should also check their stock.
Check for the NDC code 69374-979-50 on the packaging. The syringes were manufactured in lots MS2002A through MS2019A with specific expiration dates.
Immediately stop using any recalled morphine syringes as they may not be sterile and could cause infections.
The NDC code is 69374-979-50.
The syringes have expiration dates from July 2, 2022, to October 14, 2022, depending on the lot.
Look for the NDC code 69374-979-50 on the packaging and check the lot numbers MS2002A through MS2019A.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1265-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1265-2022 from Nephron. 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.
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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.
