FDA Device recall Z-1366-2015
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs…
- FDA Device
- Class II
- terminated
- Published 2015-04-08
On 2015-04-08 the FDA classified a Class II recall of Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs… by Owen Mumford Usa, citing the syringe carrier is missing components: a damper and spring.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1366-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-24 |
| Published | 2015-04-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Owen Mumford Usa |
| Distribution | US |
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.
Reason
The syringe carrier is missing components: a damper and spring.
Identifiers
| upc | 384701310010 |
|---|---|
| code_info | Lot No. 5LW |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1366-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.