SX-One MicroKnife — Class II medical device recall Z-1387-2022
Terminated recall by SONEX HEALTH LLC, reported 2022-07-27, distributed nationwide. Potential of dull blade
| Recall number | Z-1387-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SONEX HEALTH LLC, Eagan, MN, United States |
| Recall initiated | 2022-06-29 |
| Classified | 2022-07-15 |
| Reported by FDA | 2022-07-27 |
| Terminated | 2023-04-14 |
| Distributed | Nationwide (US) |
| Quantity | 3,752 devices |
| UPC / GTIN / UDI-DI | 00860002094700 |
| Lot numbers | 20013120, 20022821, 20022822, 20022823, 20022824, 20022825, 20070603, 20070604, 20080435, 20080436, 20083114, 20083115, 40051, 40052, 40472, 40473, 40892, 40893, 41460, 41584, 41585 |
| Model numbers | 600112-001 |
Product
SX-One MicroKnife
Reason for recall
Potential of dull blade
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-1387-2022. 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.