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FDAFDA · Food and drugs·Recall number D-0750-2022

Sodium Acetate Injection, USP, 400 mEq / 100 mL (4 mEq / mL), packaged in 2 trays of 20 vials per shipper (NDC 63323-032-00), each vial: 100 mL fill in a 100 mL vial (NDC 63323-032-04), Rx Only, Fresenius Kabi, Lake Zurich, IL 60047

Published March 30, 2022 · Recall initiated: March 4, 2022

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Presence of particulate matter: particulates composed of carbon and oxygen with varying amounts of iron and trace amounts of sodium, silicon, chromium, aluminum and cellulose.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
SODIUM ACETATE
Manufacturer
Fresenius Kabi USA, LLC
Distributor
Nationwide USA
Lot
Lot #: 6124193, 6124196, 6124226, Exp 05/2022; 6124532, Exp 06/2022; 6125333, Exp 12/2022; 6125678, Exp 01/2023; 6126846, Exp 08/2023
Risk classification
Class I
Area (FDA)
drug
Country
United States

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