Nephron recalls specific Rocuronium Bromide injection vials due to potential lack of sterility, which could cause infections if used. Affected products include 50 mg/5 mL syringes with lot RC2011A.
Lack of Assurance of Sterility
Nephron is recalling Rocuronium Bromide injections that may not be sterile, risking infections if used. This recall affects prescription-only products sold with specific lot numbers and expiration dates.
The product may not be sterile, meaning it could cause infections if injected. This is a serious risk for medical use, as contaminated drugs can lead to severe health issues.
Prescription patients using Rocuronium Bromide injections from Nephron. Healthcare providers handling these products are most at risk due to potential contamination.
Check for the lot number RC2011A on the packaging. The product includes 5 x 5 mL pre-filled syringes in a 6 x 5 syringe carton, with an expiration date of February 22, 2023.
Look for the lot number RC2011A and expiration date of February 22, 2023 on the packaging.
The recall states there is a lack of assurance of sterility, so it may not be safe. Do not use the product until contacted by Nephron.
The recall does not specify a remedy, so contact Nephron directly for guidance on next steps.
Check for the lot number RC2011A and expiration date of February 22, 2023 on the packaging.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0099-2023 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0099-2023 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.
