SterRx recalls midazolam injection (50mg/50mL) due to lack of sterility assurance. This could lead to infections if used improperly. Affected lots from Nov 2021 to Dec 2021.
Lack of Assurance of Sterility
SterRx is recalling midazolam injection products that may not be sterile, which could cause infections if used. This is a serious safety issue for medical use only.
The injection product lacks proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. If used in medical procedures, this could lead to infections or other serious health issues.
Healthcare professionals using this medication for medical purposes. Patients receiving injections under medical supervision are at risk if they use the recalled product.
Check the product label for the lot numbers S21131/BSP through S21170/BUB, manufactured between November and December 2021. The product is sold by SterRx in New York.
Immediately stop using any recalled midazolam injection products as they may not be sterile and could cause infections.
No, the product lacks sterility assurance and could cause infections if used. Do not use the recalled products.
Immediately stop using it and contact your healthcare provider for alternative medication.
Lots S21131/BSP through S21170/BUB, manufactured from November to December 2021.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0300-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0300-2022 from SterRx. 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.
