[Recalled] 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 — A review of complaints identified a trend fo
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| 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 |
|---|---|
| Brand / manufacturer | Cayenne Medical Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2571-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 10 October 2013 |
| EAN / barcode | 11071203 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: A review of complaints identified a trend for drills breaking.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Cayenne Medical Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.