Nephron recalls Morphine Sulfate Injection 1 mg/mL syringes due to lack of sterility assurance. This could lead to infections if used improperly. Check your NDC number for affected lots.
Lack of Assurance of Sterility
Nephron is recalling Morphine Sulfate Injection syringes because they may not be sterile. Using these could cause infections, especially in medical settings where clean injections are critical.
The syringes lack proper sterility assurance, meaning they might contain contaminants. If used for injections, this could introduce harmful bacteria into the body, leading to infections.
Healthcare professionals and patients using this medication under prescription. Those with compromised immune systems or open wounds are at higher risk of infection.
Check for NDC number 69374-979-01, lot number MS2010A, and expiration date 8/26/2022. The product is packaged in 5 x 1 mL pre-filled syringes per carton.
Look for NDC 69374-979-01, lot MS2010A, and expiration 8/26/2022 on the syringe packaging.
The recall indicates a lack of sterility assurance, so it is not safe for medical use. Do not use these syringes.
Check for NDC number 69374-979-01, lot number MS2010A, and expiration date 8/26/2022 on the syringe packaging.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe alternatives.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1268-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1268-2022 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.
