FDAClass IIJuly 24, 2019

Milrinone Lactate Injection 200 mcg recall: Sterility Concern

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…

Why was Milrinone Lactate Injection 200 mcg recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #s: 86-615-KL, Exp. 1FEB2020; 87-701-KL, Exp. 1MAR2020; 90-114-KL, Exp. 1JUN2020

Product
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…
Recalling firm
Pfizer Inc.
Quantity
58200 bags
Distribution
United States, PR, and Guam
Recall date
July 24, 2019
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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