# FDA recall Z-2571-2018

> **Cayenne Medical Inc.** · Class II · device recall initiated 2013-10-10.

## 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.

## 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.

## Key facts

- **Recall number:** Z-2571-2018
- **Recalling firm:** Cayenne Medical Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2013-10-10
- **Report date:** 2018-08-08
- **Termination date:** 2019-02-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Scottsdale, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2571-2018

## Citation

> AI Analytics. FDA recall Z-2571-2018. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-2571-2018. Source: US FDA. Licensed CC0.

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