Class II — Owen Mumford USA, Inc.
| Recalling firm | OWEN MUMFORD LTD. |
|---|---|
| Registered facility | View this company's 5 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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 |
| Product | Petfine Auto Injector, REF 3310VET |
| Quantity | 140 units |
| Distribution | FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA |
| Initiated | 2019-07-17 |
| Classified | 2019-11-01 |
| Recall number | Z-0264-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Owen Mumford USA, Inc. (Z-0264-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83465/
Alerts for OWEN MUMFORD LTD.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.