Sanofi-Aventis U.S. LLC recalls Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.15 mg (a) 2 prefilled auto injectors + 1 trainer (NDC 0024-5831-02)
Recalled June 1, 2016 · FDA recall D-0873-2016 · Sanofi-Aventis U.S
Hazard
Defective Delivery System; potential to have inaccurate dosage delivery · FDA Class I
Units
159,000 prefilled injectors
Sold at
Nationwide
Description
Defective Delivery System; potential to have inaccurate dosage delivery
Product
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
Manufacturer(s)
Sanofi-Aventis U.S. LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →