FDA Device recall Z-1510-2016
Ossur Lil Angel Vest P2 Kodel
- FDA Device
- Class II
- terminated
- Published 2016-04-27
On 2016-04-27 the FDA classified a Class II recall of Ossur Lil Angel Vest P2 Kodel by Ossur H F, citing there is a potential for partial or complete fracture of the plastic stabilizer strap on the vest.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1510-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-14 |
| Published | 2016-04-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ossur H F |
| Distribution | US |
Product
Ossur Lil Angel Vest P2 Kodel. Pediatric sized vest is a support structure used with the halo system for traumatic or chronic disorders requiring traction along the cervical spine.
Reason
There is a potential for partial or complete fracture of the plastic stabilizer strap on the vest.
Identifiers
| code_info | P/N: 545100K units from 2008 to current |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1510-2016%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.