Medical DeviceAug 8, 2018
Cayenne Medical Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a recall — FDA Z-2571-2018
A review of complaints identified a trend for drills breaking.
Class IIFDA: TerminatedCayenne Medical Inc.
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceAug 1, 2018
Cayenne Medical AperFix Femoral Implant Coring Removal Drill, labeled as the following: a recall — FDA Z-2548-2018
A review of product complaints in 2010 identified a trend for the Coring Removal Drill of premature wear and/or breakage. This recall occurred in 2013.
Class IIFDA: TerminatedCayenne Medical Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Cayenne Medical 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.