SterRx recalls 1,000 mL Succinylcholine Chloride Injection (200 mg/10mL) due to lack of sterility assurance. This injectable medication may cause infections if used improperly.
Lack of Assurance of Sterility
SterRx is recalling a specific injectable anesthetic product because it lacks proper sterility assurance. This could lead to infections if the medication is used without being properly sterilized.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If used in medical procedures, this could lead to infections in patients or healthcare workers.
Healthcare professionals who use this injectable anesthetic medication for medical procedures. Patients receiving the medication under medical supervision are not directly affected by this recall.
Check for the product name 'Succinylcholine Chloride Injection, 200 mg per 10 mL (20 mg per mL), 1,000 mL' with NDC 70324-826-01. This medication was sold by SterRx in Plattsburgh, NY starting November 2021.
Verify the product name and NDC code (70324-826-01) to confirm if you have the recalled medication.
No, the product lacks sterility assurance and could cause infections if used improperly.
Contact SterRx at 141 Idaho Avenue, Plattsburgh, NY 12903 for assistance with the recall.
The recall record does not specify a replacement option or remedy.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0307-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0307-2022 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.
