Nephron recalls Ketamine HCl injection with potential lack of sterility. Affected lots expire by 2022-10-18. Consumers should check NDC numbers and lot codes for affected products.
Lack of Assurance of Sterility
Nephron Sterile Compounding Center is recalling Ketamine HCl injection products due to a lack of assurance of sterility. This could lead to infections if the product is used. The recall affects specific lots with expiration dates up to October 2022.
The product lacks assurance of sterility, meaning it might not be free from harmful bacteria or other contaminants. If used for injections, this could cause infections in the user. The risk is particularly concerning for medical procedures where sterile products are critical.
People who have received Ketamine HCl injection from Nephron Sterile Compounding Center with the specified NDC numbers and lot codes are affected. Medical professionals using these products for injections are most at risk.
Check the NDC number 69374-511-01 on the product packaging. Look for lot codes KH2009A through KH2020A with expiration dates up to October 2022. The product is only available by prescription.
Verify the NDC number 69374-511-01 and lot codes KH2009A through KH2020A on the product packaging.
The recall indicates a lack of assurance of sterility, so the product may not be safe for use. Do not use the affected products.
Check the NDC number and lot codes to see if your product is affected. If it is, stop using it and contact Nephron Sterile Compounding Center for further instructions.
Look for the NDC number 69374-511-01 and lot codes KH2009A through KH2020A with expiration dates up to October 2022 on the product packaging.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-1261-2022 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-1261-2022 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.
