Nephron recalls Atropine Sulfate Injection syringes due to lack of sterility assurance. This could lead to infections if used improperly. Check NDC codes and expiration dates for affected lots.
Lack of Assurance of Sterility
Nephron is recalling Atropine Sulfate Injection syringes because they may not be sterile. Using these syringes could cause infections, especially in medical settings where sterility is critical.
The syringes may not be sterile, which can lead to infections if used for injections. This is particularly dangerous in medical settings where clean procedures are essential.
Healthcare professionals and patients using this medication under prescription. Those handling the syringes in medical facilities are most at risk due to potential contamination.
Check for NDC code 69374-935-03 and lots AS2001A, AS2002A, or AS2003A. The syringes expire by August 2022, August 17, 2022, or September 3, 2022 respectively.
Verify the NDC code and expiration dates to confirm if your syringes are affected.
The recall is due to a lack of assurance of sterility, which could lead to infections if the syringes are used improperly.
The official recall notice does not specify a remedy, so check with the manufacturer for further instructions.
Look for NDC code 69374-935-03 and lots AS2001A, AS2002A, or AS2003A with specific expiration dates.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1246-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1246-2022 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.
