Biomet Microfixation recalls

Biomet Microfixation has 19 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 24 May 2017.

Total recalls19since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 24 May 2017

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 19 100%Class III 0 0%

Why biomet microfixation is recalled

Product types

Other Medical Devices1579%
Surgical Instruments421%

By year

201715%
201615%
2015211%
20141579%

All biomet microfixation recalls, newest first

19 total

Reported	Class	Recall	Company	Reason	Where
24 May 2017Device	CLASS II	TraumaOne System Surgical Tray recalled by Biomet Microfixation	Biomet Microfixation	Other	AL, MO, UT
14 Sep 2016Device	CLASS II	Hard Tissue Replacement (HTR) Implant recalled by Biomet Microfixation	Biomet Microfixation	Sterility	Nationwide
28 Oct 2015Device	CLASS II	Thinflap System Case The cases hold surgical recalled	Biomet Microfixation	Other	Nationwide
28 Oct 2015Device	CLASS II	Neuro Combo Set Case The cases hold surgical recalled	Biomet Microfixation	Other	Nationwide
17 Dec 2014Device	CLASS II	Total Temporomandibular Joint Replacement System- Lft Stand recalled	Biomet Microfixation	Other	Nationwide
17 Dec 2014Device	CLASS II	Total Temporomandibular Joint Replacement System- Lft Stand recalled	Biomet Microfixation	Other	Nationwide
17 Dec 2014Device	CLASS II	Total Temporomandibular Joint Replacement System- Rt recalled	Biomet Microfixation	Other	Nationwide
17 Dec 2014Device	CLASS II	Total Temporomandibular Joint Replacement System- Rt recalled	Biomet Microfixation	Other	Nationwide
17 Dec 2014Device	CLASS II	Total Temporomandibular Joint Replacement System- Rt Stand recalled	Biomet Microfixation	Other	Nationwide
17 Dec 2014Device	CLASS II	Total Temporomandibular Joint Replacement System- Lft Narrow Ti Mand recalled	Biomet Microfixation	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.