Hospira Inc. recalls Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container…

Recall date

February 2, 2016

Source

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

Recall number

D-0727-2016

FDA classification

Class III

Brand / firm

Hospira Inc.

Sold / distributed

Nationwide and Hong Kong

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date printed on the primary container labeled "01AUG1017" rather than "01AUG2017".

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7965-09, Barcode (01) 0 030409 796509 0.