FDA Device recall Z-0633-2024
Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
- FDA Device
- Class II
- ongoing
- Published 2024-01-10
On 2024-01-10 the FDA classified a Class II recall of Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025 by Beaver Visitec International, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0633-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-10-10 |
| Published | 2024-01-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Beaver Visitec International |
| Distribution | n/a |
Product
Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
Reason
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.
Identifiers
| code_info | UDI-DI: 30886158000373; Lot Number: 6049877 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0633-2024%22
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