Xstar Kojo Safety Slit Knife — Class II medical device recall Z-0633-2024
Ongoing recall by Beaver Visitec International, Inc., reported 2024-01-10. One lot of Part Number 373025, Xstar¿ Kojo Safety Slit Knife 2.5mm 45¿ bevel up, incorrectly contains a bevel
| Recall number | Z-0633-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaver Visitec International, Inc., Waltham, MA, United States |
| Recall initiated | 2023-10-10 |
| Classified | 2024-01-04 |
| Reported by FDA | 2024-01-10 |
| Countries outside the US | JP |
| Quantity | 2,160 units |
| UPC / GTIN / UDI-DI | 30886158000373 |
| Lot numbers | 6049877 |
| Model numbers | 373025 |
Product
Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
Reason for recall
One lot of Part Number 373025, Xstar¿ Kojo Safety Slit Knife 2.5mm 45¿ bevel up, incorrectly contains a bevel down blade instead of a bevel up 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-0633-2024. 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.