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Cayenne Medical recalls

Cayenne Medical has 3 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 8 Aug 2018. The most frequent reason is device malfunction.

Total recalls3since 2018

Last 12 months0reported

Class I00% of total

Ongoing0latest 8 Aug 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why cayenne medical is recalled

Device Malfunction3100%

Product types

Hip & Knee Implants267%
Other Medical Devices133%

By year

20183100%

All cayenne medical recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
8 Aug 2018Device	CLASS II	Drill (Fluted-Hard Bone), for Quattro Link, labeled as recalled	Cayenne Medical	Device Malfunction	36 states
1 Aug 2018Device	CLASS II	AperFix Femoral Implant Coring Removal Drill recalled by Cayenne Medical	Cayenne Medical	Device Malfunction	Nationwide
18 Jul 2018Device	CLASS II	AperFix AM Femoral Implant recalled by Cayenne Medical	Cayenne Medical	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.