Reported Jul 20, 2016 · Terminated
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
Hospira Inc.
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. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
Diazepam Injection USP 10mg/2mL (5 mg/mL2 mL)Rx onlyHospira Inc. Lake ForestIL 60045NDC 0409-1273-32
- Lot codes and dates
Lot #: 52610LLExp. 01 OCT 2016Lot #: 57660LLExp. 01 MAR 2017
- Amount recalled
- 373,850 tubes
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
Crystallization: Product contains particulate identified to be crystallized active ingredient.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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