Drill — Class II medical device recall Z-2571-2018
Terminated recall by Cayenne Medical Inc., reported 2018-08-08, distributed in AK, AL, AR, AZ, CA, CO, FL, GA…. A review of complaints identified a trend for drills breaking.
| Recall number | Z-2571-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cayenne Medical Inc., Scottsdale, AZ, United States |
| Recall initiated | 2013-10-10 |
| Classified | 2018-07-28 |
| Reported by FDA | 2018-08-08 |
| Terminated | 2019-02-26 |
| Distributed | 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 |
| Quantity | 229 devies |
| Lot numbers | 10081305, 1061401, 11051503, 11071203, 11141, 11281201, 11463, 1221501, 1221502, 1221503, 2211211, 3011650, 4031303, 4071521, 4071522, 4271209, 5091601, 5091602, 59068, 59069, 6061310, 6241501, 7111613, 7181406, 7181408, 7221613, 8301608, 8301609, 9061302, 9161409, 9271618, 9271619, 9271620, 9271621, 9271623 |
| Model numbers | CM-9300, CM-9324 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2571-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.