NOREPINEPHRINE in 5% Dextrose Injection, 8 mg per 250 mL (32 mg per mL) Injection, Rx only, SterR...

FDA Recall #D-0314-2022 — Class II — November 12, 2021

Recall #D-0314-2022 Date: November 12, 2021 Classification: Class II Status: Terminated

Product Description

NOREPINEPHRINE in 5% Dextrose Injection, 8 mg per 250 mL (32 mg per mL) Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-476-01.

Reason for Recall

Lack of Assurance of Sterility

Recalling Firm

SterRx, LLC — Plattsburgh, NY

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

1428 bags

Distribution

U.S.A. Nationwide

Code Information

S21409/CCR

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated