FDA recall record

Pfizer Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection 40 mg/200 recall — FDA D-1486-2019

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

Class IIclassification
D-1486-2019official record ID
Jul 24, 2019report date

Recall record at a glance

Official recordD-1486-2019
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPfizer Inc.
Report dateJul 24, 2019
Recall initiation dateJul 9, 2019
Quantity58200 bags
LocationNew York, NY, United States

Official product description

Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection 40 mg/200 mL, 200 mL bag, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2776-02, Barcode (01)00304092776028.

Why the product was recalled

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

Distribution information

United States, PR, and Guam

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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