METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
Reported: March 1, 2017 Initiated: February 10, 2017 #D-0480-2017
Product Description
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
Reason for Recall
Lack of Sterility Assurance: customer report of leaking bag
Details
- Recalling Firm
- Hospira Inc., A Pfizer Company
- Units Affected
- 578,784 bags
- Distribution
- Nationwide and Puerto Rico
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24. Recalled by Hospira Inc., A Pfizer Company. Units affected: 578,784 bags.
Why was this product recalled? ▼
Lack of Sterility Assurance: customer report of leaking bag
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 1, 2017. Severity: Moderate. Recall number: D-0480-2017.
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