FDAFDA · Food and drugs·Recall number D-1421-2012
Epinephrine Injection, USP, 1:1000 (1 mg/mL), 25 x 1 mL Ampules, For SC and IM Use, For IV and IC Use after Dilution, Rx Only, American Regent, Inc., Shirely, NY 11967 --NDC 0517-1071-25
Published July 25, 2012 · Recall initiated: April 24, 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 Particulate Matter
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Luitpold Pharmaceuticals, Inc.
- Distributor
- Nationwide
- Lot
- Lot #1395 Exp: July 2012
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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