SterRx recalls NOREPINEPHRINE 16mg per 250mL injection due to lack of sterility assurance. This could lead to infections if used improperly. Affected units have specific NDC and batch numbers listed in the recall.
Lack of Assurance of Sterility
SterRx is recalling NOREPINEPHRINE 16 mg per 250 mL injection because it lacks sterility assurance. This means the product could cause infections if used, especially in medical settings where sterility is critical.
The injection lacks sterility assurance, meaning it could contain harmful bacteria or other contaminants. If used, this could lead to infections, especially in medical procedures where sterile conditions are essential.
Patients using this injection for medical purposes, particularly those in healthcare settings. Individuals with access to the recalled product are most at risk.
Check for the NDC number 70324-926-01 on the product label. The product was sold between November 2021 and May 2022 with specific batch numbers listed in the recall notice.
Look for the NDC number 70324-926-01 on the injection bottle.
No, the product lacks sterility assurance and could cause infections if used. Do not use this product.
Check the product label for the NDC number 70324-926-01. If it matches, stop using it and contact SterRx for instructions.
The product was recalled starting November 2021 with specific batch numbers listed in the recall notice.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0322-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0322-2022 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.
