Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Autoject EI Recalled by Owen Mumford USA, Inc. Due to There is a possible assembly error on Autoject...

Date: July 17, 2019
Company: Owen Mumford USA, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Owen Mumford USA, Inc. directly.

Affected Products

Autoject EI, REF AJ1310

Quantity: 1510 units

Why Was This 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

Where Was This Sold?

This product was distributed to 13 states: CA, CO, FL, KY, LA, MO, NH, NJ, NY, NC, PA, SC, TX

Affected (13 states)Not affected

About Owen Mumford USA, Inc.

Owen Mumford USA, Inc. has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report