Nephron recalls 5x10 pre-filled calcium gluconate syringes due to lack of sterility assurance. This could lead to infections if used improperly. Contact Nephron for details.
Lack of Assurance of Sterility
Nephron is recalling 5x10 pre-filled calcium gluconate syringes because they may not be sterile. Using these syringes could cause infections if they are contaminated.
The syringes may not be sterile, which means they could introduce harmful bacteria into the body during medical procedures. This poses a risk of infection if the syringes are used without proper sterilization.
Healthcare professionals who use these syringes for medical treatments. Patients receiving injections with these syringes are at risk of infection.
Check for the Nephron brand, 10 mL pre-filled syringes, and the lot numbers CG1003A (expiring Dec 2022) or CG2001A (expiring Feb 2023).
Look for the lot numbers CG1003A or CG2001A on the syringe carton.
The recall states there is a lack of assurance of sterility, so these syringes may not be safe for medical use.
The recall record does not specify a remedy or replacement process.
The recall record does not provide specific instructions for disposal or replacement.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0951-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0951-2022 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.
