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
December 24, 2014FDASirius Polish Cemented Stem 38C Catalog Number: 51-199335 Lot Number Identification: 14…Z-0823-2015
December 24, 2014FDADevice Brand Name: Sirius Polish Cemented Stem 34B Device Classification Name: prosthesi…Z-0822-2015
October 22, 2014FDADiscovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow …Z-0075-2015
October 15, 2014FDACompress Face Reamer Product Usage: Correction of revision of unsuccessful osteotom…Z-0021-2015
October 15, 2014FDAMamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba instruments are util…Z-0058-2015
October 15, 2014FDAGreen Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments are utilized t…Z-0057-2015
October 15, 2014FDABlack Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments are utilized t…Z-0056-2015
August 27, 2014FDAVanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORA…Z-2242-2014
August 20, 2014FDADevice Brand Name: Distal Radius Fracture Repair System Device Classification Name: Plat…Z-2212-2014
July 2, 2014FDADISCOVERY ELBOW prosthesis, 4 MM X 100 MM RIGHT HUMERAL FLANGED I BOND COAT Tl 6AL 4V ALL…Z-1925-2014
June 25, 2014FDAG7 Acetabular System Positioning Guide Rod, orthopedic surgical instrument for hip prosth…Z-1837-2014
June 25, 2014FDAG7 Acetabular System Positioning Guide Post, orthopedic surgical instrument for hip prost…Z-1838-2014
June 25, 2014FDAEZPass Passer, Sterile single use arthroscopic instrument utilized in conjunction with a …Z-1803-2014
June 25, 2014FDAEZPass Suture Retriever, Nitinol, Single Pack, Part number 10007380. Orthopedic Manual S…Z-1801-2014
June 25, 2014FDAEZPass Nylon Monofilament Single Pack, Part number 110007379, Orthopedic Manual Surgical …Z-1802-2014
May 21, 2014FDAExploR 7x26mm Modular Radial Stem, Catalog number 11-210062. Elbow prosthesis orthopedic…Z-1615-2014
March 26, 2014FDAPart 475630, Intramedullary Bone Saw, Cam Assembly Size 14 mm, The Biomet Intrame…Z-1244-2014
March 26, 2014FDAPart 475620 Intramedullary Bone Saw CAM Assembly Size 12mm, A unique and exclusive …Z-1242-2014
March 26, 2014FDAPart 475625, Intramedullary Bone Saw, Cam Assembly Size 13 mm, The Biomet Intramedu…Z-1243-2014
January 22, 2014FDALocking Cortical Screw 3.5mmX38mm REF 8161-35-038Z-0716-2014
January 1, 2014FDAG7 Acetabular Screw 6.5mmx35mm Part Number: 010001000Z-0493-2014
December 25, 2013FDAouter box: Ref 906768, CurvTek Eye Needle 22 MM X-large Stainless Steel, Single Use Gamm…Z-0523-2014
December 4, 2013FDAREF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless St…Z-0381-2014
November 27, 2013FDAJuggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Jug…Z-0364-2014
July 17, 2013FDAREF 154214 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size C3 ARCOM UHMWP…Z-1705-2013

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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