Z-0633-2024 Class II Ongoing
FDA device recall Z-0633-2024 was initiated by Beaver Visitec International, Inc. on October 10, 2023 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 2160 units.
Recall Details
- Product Type
- Devices
- Report Date
- January 10, 2024
- Initiation Date
- October 10, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2160 units
Product Description
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.
Distribution Pattern
International Distribution to Japan.
Code Information
UDI-DI: 30886158000373; Lot Number: 6049877