Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0264-2020 — Petfine Auto Injector, REF 3310VET

U.S. FDA — Device Enforcement · United States · 2019-07-17 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0264-2020
Date of alert
2019-07-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Owen Mumford USA, Inc.
Product category
device
Product type
Devices
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.