Nephron recalls 50 mg/5 mL Ketamine syringes due to lack of sterility assurance. Affected lots expire 7/20/2022. Stop using immediately to avoid infection risks.
Lack of Assurance of Sterility
Nephron is recalling certain Ketamine syringes because they may not be sterile. Using these syringes could lead to infections. Affected products were sold with specific lot numbers and expiration dates.
The syringes may not be sterile, which can cause infections if used for medical injections. This lack of sterility could lead to serious health issues if the syringes are used without proper cleaning.
Patients using Ketamine syringes from Nephron's 503B outsourcing facility in West Columbia, SC. Healthcare providers and patients who received these syringes with the listed lot numbers are most at risk.
Check for the lot numbers KH2006A, KH2006B, or KH2012B on the syringe packaging. Products expire by July 20, 2022 or August 23, 2022. The NDC code 69374-982-55 identifies these syringes.
Discard any syringes with the affected lot numbers KH2006A, KH2006B, or KH2012B.
No, these syringes may not be sterile and could cause infections. Do not use them.
The affected lot numbers are KH2006A, KH2006B, and KH2012B.
The syringes expire by July 20, 2022 for KH2006A and KH2006B, and August 23, 2022 for KH2012B.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1259-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1259-2022 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.
