Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Reported: March 6, 2013 Initiated: January 10, 2013 #D-169-2013
Product Description
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 for Recall
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Details
- Recalling Firm
- Hospira, Inc.
- Units Affected
- 63,900 vials
- Distribution
- Nationwide
- Location
- Rocky Mount, NC
Frequently Asked Questions
What product was recalled? ▼
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04. Recalled by Hospira, Inc.. Units affected: 63,900 vials.
Why was this product recalled? ▼
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 6, 2013. Severity: Moderate. Recall number: D-169-2013.
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