Class II
Terminated
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
This recall has been terminated (originally issued March 6, 2013).
- Company
- Hospira, Inc.
- Recall Initiated
- January 10, 2013
- Posted
- March 6, 2013
- Recall Number
- D-169-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 63,900 vials
- Firm Location
- Rocky Mount, NC, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Distribution
Nationwide
Lot / Code Info
18-099-DK
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