FDA recall Z-1047-2019

Avitus Orthopaedics, Inc. · Class II · device

Product

Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-210 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow

Reason for recall

Breach in the sterile barrier pouch may compromise sterility of the device.

Distribution

US Nationwide distribution to states of: AZ, CA, CT, FL, MD, MI, NM, OH and PA; and Internationally to: Brazil.

Key facts

Status
Terminated
Initiation date
2019-02-18
Report date
2019-04-03
Termination date
2020-04-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Farmington, CT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1047-2019