FDA Device recall Z-0569-2022
R82 by ETAC Push Brace for High-Low
- FDA Device
- Class II
- terminated
- Published 2022-02-16
On 2022-02-16 the FDA classified a Class II recall of R82 by ETAC Push Brace for High-Low by R82 A S, citing the chrome surface of the push brace can crack during use, potentially cutting the user.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0569-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-12-08 |
| Published | 2022-02-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | R82 A S |
| Distribution | US |
Product
R82 by ETAC Push Brace for High-Low
Reason
The chrome surface of the push brace can crack during use, potentially cutting the user.
Identifiers
| code_info | Model No. 8910545, Manufactured from 08/09/2021-10/03/2021 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0569-2022%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.