PlainRecalls
FDA Drug Moderate Class II Terminated

10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13

Reported: October 16, 2019 Initiated: October 2, 2019 #D-0136-2020

Product Description

10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13

Reason for Recall

Lack of Assurance of Sterility: Bag has the potential to leak.

Details

Recalling Firm
Pfizer Inc.
Units Affected
17832 bags
Distribution
Nationwide in the United States and Puerto Rico
Location
New York, NY

Frequently Asked Questions

What product was recalled?
10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13. Recalled by Pfizer Inc.. Units affected: 17832 bags.
Why was this product recalled?
Lack of Assurance of Sterility: Bag has the potential to leak.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 16, 2019. Severity: Moderate. Recall number: D-0136-2020.