⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Is Biomet recalled?

Biomet recalls - full list & free alerts

Official U.S. agency records list 6 recalls involving Biomet in the last 12 months, most recently on 2026-08-12. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (6)

Biomet, Inc.: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm
Medical DevicesFDA (device) · 2026-08-12 · Class II
Biomet, Inc.: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm
Medical DevicesFDA (device) · 2026-08-12 · Class II
Biomet, Inc.: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm
Medical DevicesFDA (device) · 2026-08-12 · Class II
Biomet, Inc.: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mm
Medical DevicesFDA (device) · 2026-08-12 · Class II
Biomet, Inc.: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedullary Bone Saw Blade Assembly 16mm
Medical DevicesFDA (device) · 2026-08-12 · Class II
Biomet, Inc.: BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
Medical DevicesFDA (device) · 2025-10-29 · Class II
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