Nephron recalls 50 mg/5 mL Ketamine injections due to lack of sterility assurance. Affected lots expire by June 2022. Stop using immediately if you have these syringes.
Lack of Assurance of Sterility
Nephron is recalling 50 mg/5 mL Ketamine injections that may not be sterile. This could lead to infections if used improperly. The recall affects specific lots with expiration dates up to August 2022.
The injections lack proper sterility assurance, meaning they could contain harmful bacteria. Using non-sterile injections can cause serious infections, especially in medical procedures.
People who have the recalled Ketamine injections for medical use. Those with the specific lots listed (KH1086A through KH2012A) are most at risk.
Check the product label for the lot numbers KH1086A, KH2002B, KH2008B, or KH2012A. The expiration dates range from June 2022 to August 2022.
Discard the recalled Ketamine injections if you have them. Do not use the product.
Lots KH1086A, KH2002B, KH2008B, and KH2012A with expiration dates up to August 2022.
Look for the lot numbers on the product label: KH1086A, KH2002B, KH2008B, or KH2012A.
The recall does not mention a return process, so you should discard the product immediately.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0960-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0960-2022 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.
