# FDA recall Z-0263-2020

> **Owen Mumford USA, Inc.** · Class II · device recall initiated 2019-07-17.

## Product

Autoject EI, REF AJ1310

## 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

## Distribution

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

## Key facts

- **Recall number:** Z-0263-2020
- **Recalling firm:** Owen Mumford USA, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-07-17
- **Report date:** 2019-11-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marietta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0263-2020

## Citation

> AI Analytics. FDA recall Z-0263-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0263-2020. Source: US FDA. Licensed CC0.

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