FDA Drug Recalls

Recalls / Class II

Class IID-0317-2022

Product

Fentanyl Citrate, in 0.9% Sodium Chloride Injection, 2.5 mg per 250 mL, (10 mcg per mL), Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-327-02.

Affected lot / code info
S21353/CAM 26-Mar-22 S21358/CAR 30-Mar-22 S21364/CAX 6-Apr-22

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
SterRx, LLC
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
141 Idaho Ave, Plattsburgh, New York 12903-3987

Distribution

Quantity
5000 bags
Distribution pattern
U.S.A. Nationwide

Timeline

Recall initiated
2021-11-12
FDA classified
2021-12-29
Posted by FDA
2022-01-05
Terminated
2023-12-06
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0317-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.