Nephron Sterile Compounding Center recalls 50 mg hydro morphine syringes due to lack of sterility assurance. Affected units may cause infection if used.
Lack of Assurance of Sterility
Nephron Sterile Compounding Center recalled hydro morphine syringes because they lack sterility assurance. Using these syringes could lead to infections if they are not properly sterilized.
The syringes were manufactured without proper sterility assurance, meaning they might not be clean enough for medical use. This could lead to infections if used without proper sterilization.
Healthcare professionals using these syringes for medical injections are most at risk. Patients receiving injections with these syringes could be exposed to infections.
Check for the Nephron brand, 50 mg hydro morphine syringes, and the lot number HN2002A with expiration date 7/26/2022.
Look for the Nephron brand, 50 mg hydro morphine syringes with lot number HN2002A and expiration date 7/26/2022.
No, these syringes lack sterility assurance and could cause infections if used without proper sterilization.
Check for the lot number HN2002A and expiration date 7/26/2022. If you have them, stop using and contact Nephron for guidance.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1258-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1258-2022 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.
