Owen Mumford Autoject EI Recall: Possible Assembly Error in Lot V14

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Recalling firmOwen Mumford USA, Inc.1755 W Oak Commons Ct, N/A · Marietta, GA 30062-2280

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Owen Mumford is recalling Autoject EI devices with lot number V14 because of a possible assembly error. This could lead to safety issues if the device is used incorrectly.

Why it’s dangerous

The recall states there is a possible assembly error in lot V14. This could result in the device not functioning correctly, potentially leading to safety risks during use.

Who’s affected

Owners of Autoject EI devices with lot number V14 are affected. Users of these devices are at risk if the assembly error causes improper function.

How to tell if you have this one

Check for the lot number V14 on the Autoject EI device. The product may be labeled as REF AJ1310 or branded as Petfine Auto Injector.

Brand
Owen Mumford
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Lot Number
Look for the lot number V14 on the Autoject EI device.

✎ GovInfoNow

Questions people ask

What is the specific model number for this recall?

The recall applies to Autoject EI with lot number V14.

Is there a fix for this issue?

The recall does not mention a remedy or fix.

How can I tell if my device is affected?

Check for the lot number V14 on the Autoject EI device.

Take action

Contact Owen Mumford

We’ve drafted a message you can send Owen Mumford to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0263-2020 — Owen Mumford Owen Mumford

Hello,

I own a Owen Mumford that is covered by recall Z-0263-2020 from Owen Mumford.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0263-2020 (July 17, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0263-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Owen Mumford USA, Inc. recalls Autoject EI, REF AJ1310

Recall notice