Biomet, Inc.: 120 recalls on record

Recalls filed with 1 agency: FDA (120).

First recall on record: September 26, 2012. Most recent: August 12, 2026.

Risk classification: Class II: 119 · Class III: 1

Most recent recalls

DateAgencyProduct
August 12, 2026FDAIntramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description…Z-2867-2026
August 12, 2026FDAIntramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description…Z-2869-2026
August 12, 2026FDAIntramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description…Z-2868-2026
August 12, 2026FDAIntramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description…Z-2870-2026
August 12, 2026FDAIntramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description…Z-2871-2026
November 27, 2024FDAJuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357Z-0477-2025
July 3, 2024FDARingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthr…Z-2179-2024
May 1, 2024FDAVanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. T…Z-1607-2024
November 29, 2023FDACompress Device Segmental Anchor Plug, 20 MM-For Correction of revision of unsuccessful o…Z-0375-2024
November 29, 2023FDACompress Device Short Anchor Plug, 28 MM-For Correction of revision of unsuccessful osteo…Z-0388-2024
November 29, 2023FDACompress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful o…Z-0374-2024
March 29, 2023FDAG7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 1100244…Z-1284-2023
December 30, 2020FDAVanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for us…Z-0723-2021
December 23, 2020FDASterile Trac System Thinflap 24 MM Burr Hole Plate, Item number SP-STA-1021-12 - Product …Z-0629-2021
December 23, 2020FDACustom Cancellous Thread, Item numbers CP161941, CP161943 - Product Usage: 1. Noninfla…Z-0621-2021
December 23, 2020FDA3.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Ite…Z-0616-2021
December 23, 2020FDAComprehensive Total Shoulder System/Bio-Modular Choice Shoulder System, Item number 40666…Z-0620-2021
December 23, 2020FDAOxford Fixed Lateral, Item numbers 154330, 154370, 154373 154376 - Product Usage: indica…Z-0624-2021
December 23, 2020FDAPHOENIX, Interlocking screw for IM nail, Item numbers 14-405040, 14-405042, 14-405044, 14…Z-0625-2021
October 14, 2020FDABiomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055Z-0084-2021
October 14, 2020FDABiomet Regenerex Primary Taper Cap Item Number 141269Z-0081-2021
October 14, 2020FDABiomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055Z-0083-2021
June 3, 2020FDAKnee Products: 189260 Vanguard Knee System, CR-L Mono Lock Tibial Bearing, 10 MM X 71 MM…Z-2151-2020
June 3, 2020FDAKnee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 18…Z-2154-2020
June 3, 2020FDAKnee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)008…Z-2156-2020

Questions about this company

How many recalls does Biomet, Inc. have?
Recalert has 120 U.S. recalls on record for Biomet, Inc., published between September 26, 2012 and August 12, 2026.
What was the most recent Biomet, Inc. recall?
FDA recall Z-2867-2026, published August 12, 2026: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm
Which agencies have handled Biomet, Inc. recalls?
Biomet, Inc. appears as the recalling firm in recalls from: FDA (120).

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