Cayenne Medical Inc. Recall: Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as:
Cayenne Medical Inc. Recall: Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Cayenne Medical Inc.; Product: Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-930
| Recalling firm | Cayenne Medical Inc. |
|---|---|
| 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 |
| Reason for recall | A review of complaints identified a trend for drills breaking. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | 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. |
| Recall initiated | 20131010 |
| Recall number | Z-2571-2018 |
| Category | device |
| State | AZ |
| Country | United States |
$29/mo
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