Reported Mar 6, 2013 · Terminated
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC…
Hospira, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira, Inc. · Hwy. 301 N. + 4285 North Wesleyan Blvd. · Rocky Mount, NC · 27804
Is this the product you have?
- Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
- Lot codes and dates
- 18-099-DK
- Amount recalled
- 63,900 vials
Where it was sold
- Nationwide
Why it was recalled
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
This product could cause temporary or reversible health problems — stop using it.
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