FDA Device recall Z-1030-2022
Restrata, Part Number RWM1-2X2
- FDA Device
- Class II
- terminated
- Published 2022-05-11
On 2022-05-11 the FDA classified a Class II recall of Restrata, Part Number RWM1-2X2 by Acera Surgical, citing misprinted expiration date on the shelf-box.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1030-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-03-21 |
| Published | 2022-05-11 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Acera Surgical |
| Distribution | US |
Product
Restrata, Part Number RWM1-2X2
Reason
Misprinted expiration date on the shelf-box
Identifiers
| code_info | Lot Number 51745 UDI (01) 8 52425800 60682 (10) 51745 (17) 220218 (21) 0068 |
|---|
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-1030-2022%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.