Home / Recalls / Medical Devices
Owen Mumford USA, Inc. recalls Autoject EI, REF AJ1310
Recalled November 13, 2019 · FDA recall Z-0263-2020 · Owen Mumford USA
Hazard
There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107 · FDA Class II
Units
1510 units
Sold at
FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA
Description
There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107
Product
Autoject EI, REF AJ1310
Manufacturer(s)
Owen Mumford USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →