Pfizer Inc. recalls 25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA,…

Recall date

November 27, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0577-2020

FDA classification

Class II

Brand / firm

Pfizer Inc.

Sold / distributed

Nationwide within the United States including Puerto Rico.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or expiration date.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-1775-10