Arthrosurface recalls

Arthrosurface has 6 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 30 Dec 2015.

Total recalls6since 2015

Last 12 months0reported

Class I00% of total

Ongoing0latest 30 Dec 2015

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 6 100%Class III 0 0%

Why arthrosurface is recalled

Other Reasons583%
Sterility117%

Product types

Hip & Knee Implants583%
Other Medical Devices117%

By year

20156100%

All arthrosurface recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
30 Dec 2015Device	CLASS II	Total Toe Instrument Kit, Labeled in part recalled by Arthrosurface	Arthrosurface	Sterility	CA, PA, WV
18 Feb 2015Device	CLASS II	25& 5x28mm Taper Post Fixation Component recalled by Arthrosurface	Arthrosurface	Other	Nationwide
18 Feb 2015Device	CLASS II	Athrosurface 75x31mm Taper Post Fixation Component recalled	Arthrosurface	Other	Nationwide
18 Feb 2015Device	CLASS II	5x32mm Taper Post Fixation Component recalled by Arthrosurface	Arthrosurface	Other	Nationwide
18 Feb 2015Device	CLASS II	HHXL (OVO) 6x32mm Taper Post Fixation Component recalled	Arthrosurface	Other	Nationwide
18 Feb 2015Device	CLASS II	25& 5x32mm Taper Post Fixation Component recalled by Arthrosurface	Arthrosurface	Other	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.