US Drug Recall Register
Class I · High risk Terminated Initiated Oct 28, 2015 (11 years ago)

Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.15 mg (a) 2 prefilled auto injectors…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Defective Delivery System; potential to have inaccurate dosage delivery

What was recalled

Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.15 mg (a) 2 prefilled auto injectors + 1 trainer (NDC 0024-5831-02) and (b) 1 prefilled auto injector + 1 trainer (NDC 0024-5831-00), Rx Only, Manufactured for Sanofi-Aventis US, LLC Bridgewater, NJ 08807 A Sanofi Company

Recalling firm
Sanofi-Aventis U.S. LLC
NDC code
0024-5831-02
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0873-2016

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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