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
June 3, 2020FDAKnee Products: 154335 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left, …Z-2148-2020
June 3, 2020FDAKnee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Righ…Z-2155-2020
April 29, 2020FDAComprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips, Model Number 11002…Z-1750-2020
April 15, 2020FDABIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 13 X 145 MM, 57 MM, Silicone, St…Z-1655-2020
April 15, 2020FDABIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.Z-1664-2020
April 15, 2020FDABIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 200 MM, …Z-1651-2020
April 15, 2020FDABIOMET StageOne, Shoulder Cement Spacer Mold 14 MM, 58 X 24 X 64 MM, Silicone, Sterile, I…Z-1661-2020
April 15, 2020FDABIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 200 MM, …Z-1652-2020
April 15, 2020FDABIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.Z-1638-2020
April 15, 2020FDABIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 200 MM, …Z-1650-2020
April 15, 2020FDABIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 200 MM, …Z-1649-2020
June 1, 2016FDAPerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femora…Z-1814-2016
June 1, 2016FDAVarious trauma and sports medicine instruments and implants. Screw, fixation, bone.Z-1823-2016
June 1, 2016FDAVarious trauma and sports medicine instruments and implants. cannula, surgical, general …Z-1816-2016
June 1, 2016FDAVarious trauma and sports medicine instruments and implants. Rod, fixation, intramedulla…Z-1819-2016
June 1, 2016FDAVarious trauma and sports medicine instruments and implants. Spinal interlaminal fixatio…Z-1826-2016
June 1, 2016FDAVarious trauma and sports medicine instruments and implants. Orthopedic manual surgical …Z-1827-2016
April 13, 2016FDAAll instrumentation associated with the Prelude PF Resurfacing Knee System.Z-1318-2016
January 20, 2016FDABiomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, …Z-0650-2016
July 22, 2015FDAA.L.P.S., 3.5mm x 60 mm Cortical Locking Screw. Bone fixation screwZ-2058-2015
July 15, 2015FDAA.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a …Z-2046-2015
July 8, 2015FDAGentle Threads Interference Screw 9x35mm Full Thread. An interference fixation screw …Z-1945-2015
June 17, 2015FDAUnilateral external fixation ankle clamp Product Usage: Unilateral external fixation …Z-1741-2015
June 17, 2015FDAComprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Stand…Z-1755-2015
February 25, 2015FDAMallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Rin…Z-1122-2015

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.
Which agencies have handled Biomet, Inc. recalls?
Biomet, Inc. appears as the recalling firm in recalls from: FDA (120).

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