SterRx recalls epinephrine injections due to lack of assurance of sterility. This could lead to infections if used improperly. Affected products include specific lot numbers and dates.
Lack of Assurance of Sterility
SterRx is recalling epinephrine injections that may not be sterile, which could cause infections if used. This is a serious risk for people who need the medication during emergencies.
The injections lack assurance of sterility, meaning they might contain harmful bacteria. Using non-sterile injections can lead to infections, especially in critical medical situations.
People with prescriptions for epinephrine injections are affected. Those who have the specific lot numbers or dates listed are at highest risk.
Check the product label for the lot numbers: S21254, S21263, S21333, or S21398. The products were sold between November 2021 and February 2022.
Immediately stop using the recalled epinephrine injections if you have them.
The product lacks assurance of sterility, which could lead to infections if used.
The affected lot numbers are S21254, S21263, S21333, and S21398.
These products were sold between November 2021 and February 2022.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0308-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0308-2022 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.
