Reported Aug 8, 2018 · Terminated
Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…
Cayenne Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Cayenne Medical Inc. · 16597 N 92nd St Ste 101 · Scottsdale, AZ · 85260-1847
Is this the product you have?
- Drill (Fluted-Hard Bone), for Quattro Link 2.9mm
- labeled as
a. Quattro Spade Drillfor 2.9mmModel Number CM-9300b. Quattro Drill 2.4mmHard BoneModel Number CM-9324
- Lot codes and dates
4 of 4 products
Products covered by this recall Model / number Product as published CM-9300— — Lot Number 2211211, 4271209, LNR, 7181408, 1221502, 4071521, 5091602, 7221613, 8301608, 9271623, 9271619, 9271621, 59068, 59069; b. CM-9324— — Lot Number LNR, LRN, 11071203, 11281201, 4031303, 6061310, 9061302, 10081305, 1061401, 7181406, 9161409, 1221503, 1221501, 4071522, 6241501, 11051503, 3011650, 5091601, 7111613, 8301609, 9271618, 9271620, 11463, 11141 - Amount recalled
- 229 devies total
Where it was sold
Why it was recalled
A review of complaints identified a trend for drills breaking.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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