PlainRecalls
FDA Drug Moderate Class II Terminated

Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 mL, 100 mL bag, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2776-23, Barcode (01)00304092776233.

Reported: July 24, 2019 Initiated: July 9, 2019 #D-1487-2019

Product Description

Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 mL, 100 mL bag, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2776-23, Barcode (01)00304092776233.

Reason for Recall

Lack of Assurance of Sterility: Bags have the potential to leak.

Details

Recalling Firm
Pfizer Inc.
Units Affected
280340 bags
Distribution
United States, PR, and Guam
Location
New York, NY

Frequently Asked Questions

What product was recalled?
Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 mL, 100 mL bag, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2776-23, Barcode (01)00304092776233.. Recalled by Pfizer Inc.. Units affected: 280340 bags.
Why was this product recalled?
Lack of Assurance of Sterility: Bags have the potential to leak.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 24, 2019. Severity: Moderate. Recall number: D-1487-2019.