SterRx recalls 250mL norepinephrine bags with potential lack of sterility. This could cause infections if used improperly. Check NDC 70324-552-01 and lot numbers for affected products.
Lack of Assurance of Sterility
SterRx is recalling norepinephrine injection products due to a lack of sterility assurance. This could lead to infections if the product is used without proper sterilization. Patients and healthcare providers should avoid using these products until a replacement is obtained.
The product lacks assurance of sterility, meaning it could be contaminated with bacteria. If used without proper sterilization, this could lead to infections in patients. The risk is particularly concerning for medical procedures where sterile solutions are critical.
Patients and healthcare providers who have received the recalled norepinephrine products. Those using the specific lot numbers listed in the recall are most at risk.
Check for the product name 'Norepinephrine 4 mg per 250 mL (16 mcg per mL) in 0.9% Sodium Chloride' in single-dose bags. Look for the NDC code 70324-552-01 and specific lot numbers listed in the recall.
Identify the product by checking the NDC code 70324-552-01 and the lot numbers listed in the recall.
The recall states there is a lack of assurance of sterility, so it is not safe to use. The product should be discarded or replaced with a non-recalled product.
If you have the recalled product, stop using it and contact SterRx at 141 Idaho Ave., Plattsburgh, NY 12903 for further instructions.
Check the NDC code 70324-552-01 and the lot numbers listed in the recall (e.g., 490062, 490151, etc.).
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0931-2023 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0931-2023 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.
