Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride, 8 mg, 250 mL excel b...

FDA Recall #D-0708-2022 — Class II — March 14, 2022

Recall #D-0708-2022 Date: March 14, 2022 Classification: Class II Status: Terminated

Product Description

Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride, 8 mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-475-15

Reason for Recall

Defective container

Recalling Firm

Athenex Pharma Solutions, LLC — Clarence, NY

Classification

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

Product Type

Drugs

Product Quantity

9,800 bags

Distribution

USA nationwide.

Code Information

Lot #: F2101639, F2101642, F2101644, F2101645, Exp 4/30/22; F2101674, F2101675, F2101676, Exp 5/05/22; F2101790, F2101791, F2101792, F2101793, F2101794, Exp 5/26/22; F2101813, Exp 5/29/22

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated