SterRx recalls NOREPINEPHRINE 8 mg per 250 mL injection (Rx only) due to lack of sterility assurance. This may cause infections if used improperly.
Lack of Assurance of Sterility
SterRx is recalling NOREPINEPHRINE 8 mg per 250 mL injections (Rx only) because they lack sterility assurance. Using these injections could lead to infections if not handled properly.
The injections were manufactured without proper sterility assurance, meaning they could contain harmful bacteria. If used, this could lead to infections, especially in patients with weakened immune systems.
Prescription patients using NOREPINEPHRINE injections for medical purposes. Those with compromised immune systems are at slightly higher risk.
Check for the product name 'NOREPINEPHRINE, 8 mg per 250 mL, (32 mcg per mL) in 0.9% Sodium Chloride Injection' with the NDC number 70324-676-01. The product was sold from November 2021 to April 2022.
Look for the product name and NDC number 70324-676-01 on the label.
No, the product lacks sterility assurance and could cause infections if used. Do not use this product.
Check for the product name 'NOREPINEPHRINE, 8 mg per 250 mL, (32 mcg per mL) in 0.9% Sodium Chloride Injection' with NDC 70324-676-01. The product was sold from November 2021 to April 2022.
Do not use this product. Contact your healthcare provider for alternative treatment options.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0321-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0321-2022 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.
