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
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Contact the company
📍Recalling firmOwen Mumford USA, Inc.1755 W Oak Commons Ct · Marietta, GA 30062-2280
“Owen Mumford Autoject EI Recall: Possible Assembly Error in Lot V14.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67401-owen-mumford-autoject-ei-recall-possible-assembly-error-in-lot. Based on FDA recall #Z-0263-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0263-2020%22&limit=1).
Owen Mumford USA, Inc. recalled Autoject EI (REF AJ1310) due to a possible assembly error in lot V14, the FDA said on July 17, 2019. The recall affects 1,510 units distributed across multiple states.
How to tell if you have it
Brand: Owen Mumford
Product: Autoject EI, REF AJ1310
Lot/Unit Number: V14
Quantity: 1,510 units
The hazard
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.
Context
GovInfoNow's records show Owen Mumford USA, Inc. has two other recalls on record since November 6, 2017, including a May 26, 2021 recall for Unifine Pentips Plus 4mm Needles mixed with 8mm Needles and a November 6, 2017 recall regarding water risk compromising sterility in Unifine Pentips 5mm x 31G Pen Needles. Other recent recalls of similar products include Olympus OER-ELITE Endoscope Reprocessor Connecting Tubes Recall (March 25, 2026), Philips Azurion 7 B20 System Recall (January 26, 2026), and Tobii Dynavox TD Navio Maxi Speech Device Recall (July 8, 2026).
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
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA
Recall number
Product, codes & lots
Quantity
Z-0263-2020
Autoject EI, REF AJ1310; Lot/Unit Number: V14
1510 units
Z-0264-2020
Petfine Auto Injector, REF 3310VET; batches V14.V976 and V14.W107
140 units
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.
Where it went and when
Where it was distributed
Distributed in 13 states.
Listed by the agency
Not listed
FDA distribution: “FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Florida, Kentucky, Louisiana, Missouri, New Hampshire, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Texas.
Recall timeline
FDA published this recall 4 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.