Medical device recalls Moderate risk

Owen Mumford USA, Inc. recalls Petfine Auto Injector, REF 3310VET

Recall date
July 17, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0264-2020
FDA classification
Class II
Brand / firm
Owen Mumford USA, Inc.
Sold / distributed
FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Petfine Auto Injector, REF 3310VET

Get recall alerts

Free email alert whenever Owen Mumford USA, Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Owen Mumford USA, Inc.