Recall: D-169-2013

Class II - Potentially Harmful

Class IIClassification

2013-01-10Initiated

TerminatedStatus

Hospira, Inc.Firm

Product

Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04

Reason

Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial

Distribution

Nationwide

Source: FDA drug enforcement report via openFDA (Voluntary: Firm initiated). If you take this product, talk to your pharmacist or doctor before stopping it.