Owen Mumford USA, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0263-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Autoject EI, REF AJ1310

Product Classification:

Class II

Date Initiated: July 17, 2019

Date Posted: November 13, 2019

Recall Number: Z-0263-2020

Event ID: 83465

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1510 units

Code Information:

Lot/Unit Number: V14

Distribution Pattern:

FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA

Voluntary or Mandated:

Voluntary: Firm initiated