Nephron recalls epinephrine syringes due to lack of sterility assurance. These pre-filled syringes may cause infections if used. Check NDC 69374-544-10 and expiration dates for affected lots.
Lack of Assurance of Sterility
Nephron is recalling epinephrine syringes that may not be sterile, posing infection risks. This is serious because medical injections require strict sterility to prevent infections.
The syringes lack proper sterility assurance, meaning they could be contaminated with bacteria. If injected, this could cause serious infections or even death in vulnerable individuals.
People with prescriptions for epinephrine injections, especially those using the recalled syringes for emergencies. Anyone with the NDC 69374-544-10 syringes from the listed lots is at risk.
Check for NDC 69374-544-10 on the syringe packaging. Look for lots EN2001A through EN2012A with expiration dates up to September 1, 2022.
Immediately discard any recalled epinephrine syringes with the listed NDC and lots.
No, the recalled syringes lack sterility assurance and could cause infections if used.
Check the NDC code 69374-544-10 and lot numbers EN2001A through EN2012A with expiration dates up to September 1, 2022.
Discard them immediately and contact Nephron at 4500 12th Street Extension, West Columbia SC 29172 for replacement.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1250-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1250-2022 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.