Biomet, Inc. recalls

All Biomet, Inc. recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (8).

8 recalls published between November 27, 2024 and August 12, 2026. Most common issues: sterility (5).

• Intramedullary Bone Saw Blade Assembly Model recall
  FDA August 12, 2026 · Biomet, Inc. · Class II
• Intramedullary Bone Saw Blade Assembly Model recall
  FDA August 12, 2026 · Biomet, Inc. · Class II
• Intramedullary Bone Saw Blade Assembly Model recall
  FDA August 12, 2026 · Biomet, Inc. · Class II
• Intramedullary Bone Saw Blade Assembly Model recall
  FDA August 12, 2026 · Biomet, Inc. · Class II
• Intramedullary Bone Saw Blade Assembly Model recall
  FDA August 12, 2026 · Biomet, Inc. · Class II
• BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model recall
  FDA October 29, 2025 · Biomet, Inc. · Class II
• Juggerknot Mini Soft Anchors, Model recall
  FDA October 1, 2025 · Biomet, Inc. · Class II
• JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357 recall
  FDA November 27, 2024 · Biomet, Inc. · Class II