Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of complaints identified a trend for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cayenne Medical Inc. directly.
Affected Products
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
Quantity: 229 devies total
Why Was This Recalled?
A review of complaints identified a trend for drills breaking.
Where Was This Sold?
This product was distributed to 36 states: AL, AK, AZ, AR, CA, CO, FL, GA, ID, IL, IN, IA, KS, MD, MA, MI, MN, MO, MT, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
About Cayenne Medical Inc.
Cayenne Medical Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report