Reported Jan 9, 2013 · Terminated
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
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?
- Epinephrine Injection USP, 1 mL
- USP 11000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
- Lot codes and dates
Lot 100953AExp 01OCT2013Lot 120803A Exp 01DEC2013
- Amount recalled
- 361,600/1-mL ampules
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Presence of Particulates; may contain glass particles
This product could cause temporary or reversible health problems — stop using it.
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