Restrata — Class II medical device recall Z-1030-2022
Terminated recall by Acera Surgical Inc, reported 2022-05-11, distributed nationwide. Misprinted expiration date on the shelf-box
| Recall number | Z-1030-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Acera Surgical Inc, Woodstock, GA, United States |
| Recall initiated | 2022-03-21 |
| Classified | 2022-05-02 |
| Reported by FDA | 2022-05-11 |
| Terminated | 2024-08-20 |
| Distributed | Nationwide (US) |
| Quantity | 83 units |
| Lot numbers | 51745 |
| Model numbers | RWM1-2X2 |
Product
Restrata, Part Number RWM1-2X2
Reason for recall
Misprinted expiration date on the shelf-box
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1030-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.