Nephron recalls 5-pack of ketamine syringes due to potential contamination. Stop using if you have these specific lot numbers.
Lack of Assurance of Sterility
Nephron is recalling a specific batch of ketamine syringes because they may not be sterile. This could lead to infections if used improperly.
The syringes may not be sterile, which can cause infections if injected. This is a serious risk for medical use, but the exact mechanism isn't clearly described in the recall.
People who have the specific lot number KH2008A of ketamine syringes from Nephron. Healthcare providers using these syringes for medical purposes are most at risk.
Check for the lot number KH2008A on the syringe carton. The product was sold by Nephron with NDC 69374-982-33 and expired 8/8/2022.
Look for the lot number KH2008A on the syringe carton to confirm if it's recalled.
The recall states there is a risk of contamination, so it is not safe to use. The manufacturer recommends checking the lot number.
The recall does not specify a remedy, so you should stop using it and contact the manufacturer for further instructions.
Check for the lot number KH2008A on the syringe carton. The product was sold by Nephron with NDC 69374-982-33 and expired 8/8/2022.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0959-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0959-2022 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.
