METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)
Reported: March 27, 2013 Initiated: February 15, 2013 #D-206-2013
Product Description
METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)
Reason for Recall
Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 567,624 bags
- Distribution
- Nationwide.
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24). Recalled by Hospira Inc.. Units affected: 567,624 bags.
Why was this product recalled? ▼
Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 27, 2013. Severity: Moderate. Recall number: D-206-2013.
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