FDAFDA · Food and drugs·Recall number D-106-2013
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Published January 9, 2013 · Recall initiated: October 25, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulates; may contain glass particles
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot 100953A, Exp 01OCT2013; Lot 120803A Exp 01DEC2013
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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