D-0323-2022 Class II Terminated
FDA drug recall D-0323-2022 was initiated by SterRx, LLC on November 12, 2021 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated December 6, 2023). Affected quantity: 20640 bags.
Recall Details
- Product Type
- Drugs
- Report Date
- January 5, 2022
- Initiation Date
- November 12, 2021
- Termination Date
- December 6, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 20640 bags
Product Description
PHENYLephrine HCl, 40 mg per 250 mL, (160 mcg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-252-01.
Reason for Recall
Lack of Assurance of Sterility
Distribution Pattern
U.S.A. Nationwide
Code Information
S21087/BQX 16-Dec-21 S21151/BTJ 24-Jan-22 S21186/BUQ 14-Feb-22 S21189/BUS 16-Feb-22 S21266/BXJ 3-Apr-22 S21307/BYW 24-Apr-22 S21313/BZC 27-Apr-22