PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: December 18, 2019 Initiated: November 27, 2019 #D-0577-2020

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Pfizer Inc.
Units Affected
77,100 syringes
Distribution
Nationwide within the United States including Puerto Rico.
Location
New York, NY

Frequently Asked Questions

What product 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. Recalled by Pfizer Inc.. Units affected: 77,100 syringes.
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or expiration date.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 18, 2019. Severity: Moderate. Recall number: D-0577-2020.