US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 24, 2012 (14 years ago)

Epinephrine Injection, USP, 1:1000 (1 mg/mL), 25 x 1 mL Ampules, For SC and IM Use, For…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Particulate Matter

What was recalled

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

Recalling firm
Luitpold Pharmaceuticals, Inc.
NDC code
0517-1071-25
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1421-2012

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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