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. 7 were reported in the last 12 months.
Total recalls279since 2012
Last 12 months7reported
Class I00% of total
Ongoing36latest 12 Aug 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 275 99%Class III 4 1%
Why biomet is recalled
Product types
By year
Ongoing biomet recalls
36 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | 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 |
|---|---|---|---|---|---|
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | ZipTight, Acute AC Joint Implant, Single Ziploop recalled by Biomet | Biomet | Other | IN |
| Device | CLASS II | Juggerknot Mini Soft Anchors recalled by Biomet | Biomet | Other | Nationwide |
| Device | CLASS II | JuggerLoc/ToggleLoc Drill Guide recalled by Biomet | Biomet | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | RingLoc Bi-Polar Hip System Acetabular Cup Outer Diameter recalled | Biomet | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Vanguard Knee System AS Tibial Bearing / DCM ArCom recalled by Biomet | Biomet | Packaging Defects | 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.