Owen Mumford USA, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1366-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: November 24, 2014

Date Posted: April 8, 2015

Recall Number: Z-1366-2015

Event ID: 70665

Reason for Recall:

The syringe carrier is missing components: a damper and spring.

Status: Terminated

Product Quantity: 3,100

Code Information:

Lot No. 5LW

Distribution Pattern:

US nationwide distribution in the states of AL, AR, CA, FL, GA, IL, MO, NC, OK, TN, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated