Z-0227-2022 Class II Ongoing
FDA device recall Z-0227-2022 was initiated by Beaver Visitec International, Inc. on October 8, 2021 and is designated Class II. Reason for recall: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades The recall status is ongoing. Affected quantity: 5950 eaches.
Recall Details
- Product Type
- Devices
- Report Date
- November 24, 2021
- Initiation Date
- October 8, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5950 eaches
Product Description
Beaver Xstar Crescent Knife, 2.5mm, 55 degrees, bevel down. Intended for or cataract surgery. REF#: 373809
Reason for Recall
Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades
Distribution Pattern
Nationwide Foreign: Australia Austria France Germany Netherlands Spain Japan Russia South Africa UK
Code Information
LOT#: 6000842, 6002045, 6011609, 6034238, 6040517, 6042907. UDI: " Primary: 00886158000594 " Secondary: 30886158000595 " Tertiary: 50886158000599