Reported Mar 1, 2017 · Terminated
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira…
Hospira Inc., A Pfizer Company
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., A Pfizer Company · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- 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
- Lot codes and dates
- Lot
54-054-JT6/1/2017
- Lot
- Amount recalled
- 578,784 bags
Where it was sold
- Nationwide
- PR
Why it was recalled
Lack of Sterility Assurance: customer report of leaking bag
This product could cause temporary or reversible health problems — stop using it.
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