FDAOctober 28, 2015drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Defective Delivery System; potential to have inaccurate dosage delivery

What to do

FDA enforcement status: Terminated

Brands named

sanofi aventis u ssanofisanofi aventis

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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 — Recall Details · AllClear