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Owen Mumford USA, Inc. recalls Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by pa
Recalled April 8, 2015 · FDA recall Z-1366-2015 · Owen Mumford USA
Hazard
The syringe carrier is missing components: a damper and spring. · FDA Class II
Units
3,100
Sold at
US nationwide distribution in the states of AL, AR, CA, FL, GA, IL, MO, NC, OK, TN, and TX.
Description
The syringe carrier is missing components: a damper and spring.
Product
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.
Manufacturer(s)
Owen Mumford USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →