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 | Terminated |
| Reason | The syringe carrier is missing components: a damper and spring. |
| Product | Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor. |
| Quantity | 3,100 |
| Distribution | US nationwide distribution in the states of AL, AR, CA, FL, GA, IL, MO, NC, OK, TN, and TX. |
| Initiated | 2014-11-24 |
| Classified | 2015-04-02 |
| Terminated | 2017-07-31 |
| Recall number | Z-1366-2015 |
| 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-1366-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70665/
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