Home / Recalls / SterRx, LLC / D-0934-2023

D-0934-2023 Class II Terminated

Recalled by SterRx, LLC — Plattsburgh, NY

FDA drug recall D-0934-2023 was initiated by SterRx, LLC on Jul 7, 2023 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated Jul 8, 2024). Affected quantity: 2,088 bags.

Recall Details

Product Type: Drugs
Report Date: Jul 26, 2023
Initiation Date: Jul 7, 2023
Termination Date: Jul 8, 2024
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 2,088 bags

Product Description

Norepinephrine 32 mg per 250 mL (128 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-702-01.

Reason for Recall

Lack of Assurance of Sterility

Distribution Pattern

Nationwide in the USA

Code Information

Lot #: 490100, Exp 27-Jul-23

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0934-2023
openFDA file date: Nov 3, 2026
Loaded by RegDataLab: Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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