Biomet recalls

Biomet has 279 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 12 Aug 2026. 36 are still ongoing. 6 were reported in the last 12 months.

Total recalls279since 2012

Last 12 months6reported

Class I00% of total

Ongoing36latest 12 Aug 2026

Recalls per month, last 24 months

click a bar for that month

1Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 2 0Nov 0 0 0Feb 0 0 0May 0 0 5Aug 0 0

Severity split

Class I 0 0%Class II 275 99%Class III 4 1%

Why biomet is recalled

Product types

By year

202652%
202521%
202431%
2023269%
2022124%
2021197%
20209735%
201810%
2016228%
2015228%

Ongoing biomet recalls

36 active

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
29 Oct 2025Device	CLASS II	ZipTight, Acute AC Joint Implant, Single Ziploop recalled by Biomet	Biomet	Other	IN

All biomet recalls, newest first

279 total

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
12 Aug 2026Device	CLASS II	Intramedullary Bone Saw Blade Assembly recalled by Biomet	Biomet	Sterility	IN
29 Oct 2025Device	CLASS II	ZipTight, Acute AC Joint Implant, Single Ziploop recalled by Biomet	Biomet	Other	IN
1 Oct 2025Device	CLASS II	Juggerknot Mini Soft Anchors recalled by Biomet	Biomet	Other	Nationwide
27 Nov 2024Device	CLASS II	JuggerLoc/ToggleLoc Drill Guide recalled by Biomet	Biomet	Packaging Defects	Nationwide
3 Jul 2024Device	CLASS II	RingLoc Bi-Polar Hip System Acetabular Cup Outer Diameter recalled	Biomet	Potency & Assay	Nationwide
1 May 2024Device	CLASS II	Vanguard Knee System AS Tibial Bearing / DCM ArCom recalled by Biomet	Biomet	Packaging Defects	Nationwide
27 Dec 2023Device	CLASS II	Biolox Ceramic Option Head Zimmer 12/14 recalled by Biomet	Biomet	Packaging Defects	9 states
27 Dec 2023Device	CLASS II	Biolox Ceramic Option Head Zimmer 12/14 +0 recalled by Biomet	Biomet	Packaging Defects	9 states
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-Correction of revision recalled	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug -For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug- Correction of revision recalled	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Segmental Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	Nationwide
29 Nov 2023Device	CLASS II	Compress Device Short Anchor Plug-For Correction recalled by Biomet	Biomet	Foreign Material	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.