SterRx recalls Fentanyl Citrate injection due to lack of sterility assurance. This medication may be contaminated, posing a risk of infection. Affected units have specific NDC numbers and were distributed in New York.
Lack of Assurance of Sterility
SterRx is recalling a specific fentanyl injection product because it may not be sterile. Using this medication could lead to infections, especially since it's a potent opioid prescribed for medical use.
The injection product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. This poses a risk of infection when administered, particularly given the medication's potency and medical use.
Prescribers and patients using the recalled fentanyl injection for medical purposes. Those with the specific NDC number 70324-327-02 are most at risk.
Check the product label for the NDC number 70324-327-02. The medication was distributed in New York starting March 2022. It's a prescription-only fentanyl injection for medical use.
Look for the NDC number 70324-327-02 on the medication label.
No, the product lacks sterility assurance and may be contaminated, posing a risk of infection.
The recall does not specify a remedy, so contact your healthcare provider for guidance.
Check the product label for the NDC number 70324-327-02. The medication was distributed in New York starting March 2022.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0317-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0317-2022 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.
