FDA recall Z-0227-2022

Beaver Visitec International, Inc. · Class II · device

Product

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

Nationwide Foreign: Australia Austria France Germany Netherlands Spain Japan Russia South Africa UK

Key facts

Status
Ongoing
Initiation date
2021-10-08
Report date
2021-11-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Waltham, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0227-2022