Avitus Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone recall — FDA Z-1046-2019
Breach in the sterile barrier pouch may compromise sterility of the device.
Overview of recall records associated with Avitus Orthopaedics, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Breach in the sterile barrier pouch may compromise sterility of the device.
Breach in the sterile barrier pouch may compromise sterility of the device.
This page summarizes recall records in which the official source identifies Avitus Orthopaedics, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.