Every recall we track for Biomet — 24 in all — plus the complaints and injury reports the public filed about them.
Biomet recalls 6.5 Cannulated Screw Taps (Item 110008466) due to incomplete design history files. These bone fixation screws are intended for temporary use during healing. Affected units have specific lot numbers.
Biomet recalls a specific proximal humerus plating system due to design history files not being completed before distribution. This affects certain surgical implants used in fracture repair. Consumers should contact Biomet for details.
Biomet recalls a specific orthopedic plate for temporary fracture fixation due to incomplete design history files before distribution. This affects certain surgical implants used in bone repair procedures.
Biomet recalls a specific proximal humerus plate model due to incomplete design history files. Affected users should contact Biomet for details on next steps.
Biomet recalls a specific proximal humerus plating system due to incomplete design history files before distribution. Affected items may pose risks during surgical use. Contact Biomet for details.
Biomet recalls a 2.7mm drill block guide sleeve for proximal humerus plating systems due to incomplete design history files. This device is used in fracture stabilization during healing. Affected units include specific lot numbers.
Biomet recalls a 140mm proximal humerus plate template for incomplete design history files. This device is used for temporary fracture stabilization. Affected units were distributed without proper design documentation.
Biomet recalls a specific proximal humerus plating system due to incomplete design history files before distribution. This may pose risks during surgical procedures. Affected patients should contact Biomet for details.
Biomet recalls drill block set screws for proximal humerus plating systems due to incomplete design history files. Affected items may pose risks during surgical procedures.
Biomet recalls a specific proximal humerus plating system due to incomplete design history files before distribution. This may affect surgical implants used in fracture repair. Affected units require verification of lot numbers and item numbers.
Biomet recalls a specific proximal humerus plate model due to incomplete design history files before distribution. This may pose risks during surgical procedures. Affected patients should contact Biomet for guidance.
Biomet recalls a proximal humerus plate template due to incomplete design history files. This may affect surgical implants used in fracture repair. Affected units were distributed without proper documentation.
Biomet recalls 8.0 Cannulated Screw Tap-Bone fixation screws (item 110008467) due to incomplete design history files. These screws are intended for temporary fracture stabilization during healing.
Biomet recalls A.L.P.S. T15 cortical screws due to incomplete design history files. This affects temporary fracture fixation devices sold for medical use. Consumers should contact Biomet for details.
Biomet recalls a specific proximal humerus plating system for temporary fracture fixation due to incomplete design history files. Affected items have a unique item number and lot number. Consumers should contact Biomet for details.
Biomet recalls 3.2mm calibrated drill bit for proximal humerus plating system due to incomplete design history files. Affected units may pose risks during surgical procedures.
Biomet recalls A.L.P.S. Proximal Humerus Plate (11-hole, 190mm) due to incomplete design history files before distribution. Affected units sold before Dec 31, 2026.
Biomet recalls a specific proximal humerus plating system due to incomplete design history files before distribution. This may affect surgical implants used in fracture stabilization.
Biomet recalls 90mm proximal humerus plate template for missing design history files. This could affect surgical safety during fracture repair. Contact Biomet for details.
Biomet recalls a specific proximal humerus plating system for temporary fracture fixation due to incomplete design history files. Affected units may have safety risks during surgical use.
Biomet recalls A.L.P.S. T15 Multi-Directional Locking Screws due to incomplete design history files. This may affect surgical implants used in fracture stabilization. No action is required as the product is not yet in use.
Biomet recalls 3.2mm drill block guide sleeve for proximal humerus plating system due to incomplete design history files. This may affect surgical implants used in fracture stabilization.
Biomet recalls all lots of Orthopedic Manual Surgical Instruments with Outer Sheaths 4.5/5.0,6.5 due to potential failure in steam sterilization validation testing.
Biomet recalls surgical tray product code 246111003 due to failed steam sterilization validation. All units are affected. Consumers should contact Biomet for details.
