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Cayenne Medical Inc. recalls Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-93
Recalled August 8, 2018 · FDA recall Z-2571-2018 · Cayenne Medical
Hazard
A review of complaints identified a trend for drills breaking. · FDA Class II
Units
229 devies total
Sold at
US distribution to AK, AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.
Description
A review of complaints identified a trend for drills breaking.
Product
Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300; b. Quattro Drill 2.4mm, Hard Bone, Model Number CM-9324
Manufacturer(s)
Cayenne Medical Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →