SterRx, LLC: Drug Recall

Recall #D-0933-2023 · 07/07/2023

Class II: Risk

Recall Details

Recall Number
D-0933-2023
Classification
Class II
Product Type
Drug
Recalling Firm
SterRx, LLC
Status
Terminated
Date Initiated
07/07/2023
Location
Plattsburgh, NY, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
92,148 bags

Reason for Recall

Lack of Assurance of Sterility

Product Description

Norepinephrine 16 mg per 250 mL (64 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per carton, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-602-01.

Distribution Pattern

Nationwide in the USA

Other Recalls by SterRx, LLC

View all recalls by SterRx, LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.