Biomet Recalls
279 recalls on record · September 26, 2012 to August 12, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 24, 2020Medical DevicesFDA
Biomet recalls Biomet Screw Instrument Tray 6.5/80MM- Surgical Tray Product Code: 246111003
Hazard: Device and tray that houses the device did not pass steam sterilization process validation testing
June 24, 2020Medical DevicesFDA
Biomet recalls Biomet Outer Sheath 4.5/5.0,6.5- Orthopedic Manual Surgical Instrument Product Code: 14235
Hazard: Device and tray that houses the device did not pass steam sterilization process validation testing
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 14 HOLE 234MM, Item Number: 110030409 - Product Usage: Intend
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 11 HOLE 197MM, Item Number: 110030408 - Product Usage: Intend
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 7 HOLE 140MM, Item Number: 110030407 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 14 HOLE 234MM, Item Number: 110030309 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 11 HOLE 197MM, Item Number: 110030308 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 7 HOLE 140MM, Item Number: 110030307 - Product Usage: Intended
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 14 HOLE 227MM, Item Number: 110030209 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 11 HOLE 190MM, Item Number: 110030208 - Product Usage: Intend
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 14 HOLE 227MM, Item Number: 110030109 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 11 HOLE 190MM, Item Number: 110030108 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE 234MM Item Number: 110025473 - Product Usag
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE 140MM Item Number: 110025472 - Product Usa
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE 90MM, Item Number: 110025471 - Product Usa
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 60MM , Item Number: 110025460 - Product Usage: Intended for
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. T15 Multi-Directional Locking Screw 3.5mm x 60mm, Item Number: 110017960 - Product Usage: Intended for temporar
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM CALIBRATED DRILL BIT, Item Number: 110017737 - Product Usage: Intended f
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. T15 LOW PROFILE CORTICAL SCREW 3.5mm x 28mm, Item Number: 110017628 - Product Usage: Intended for temporary in
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 2.7MM, Item Number: 110017563 - Product Usage: Intend
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM, Item Number: 110017553 - Product Usage: Intende
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK SET SCREW, Item Number: 110017551 - Product Usage: Intended for te
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls Biomet 8.0 Cannulated Screw Tap-Bone fixation screw Item Number: 110008467 - Product Usage: Intended for temporary inte
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet recalls Biomet 6.5 Cannulated Screw Tap - Bone fixation screw, Item Number: 110008466 - Product Usage: Intended for tempora
Hazard: Distributed to the field without having completed design history files or design transfer activities
June 17, 2020Medical DevicesFDA
Biomet, Inc. recalls Comprehensive VRS Inserter, shoulder prosthesis, Item No. 110019068. UDI: (01)00880304829503 (10)814100, (01)0088030482
Hazard: The product is being recalled due to the central screw drill seizing inside the Comprehensive VRS Inserter, which may lead to an extension of surgery to find a replacement device.
June 3, 2020Medical DevicesFDA
Biomet, Inc. recalls Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550
Hazard: Potential presence of elevated endotoxin levels that exceed the specification limit
June 3, 2020Medical DevicesFDA
Biomet, Inc. recalls Knee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Right Medial/Left Lateral, B8 US15
Hazard: Potential presence of elevated endotoxin levels that exceed the specification limit
June 3, 2020Medical DevicesFDA
Biomet, Inc. recalls Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 184764 Knees Vanguard Knee Syste
Hazard: Potential presence of elevated endotoxin levels that exceed the specification limit
June 3, 2020Medical DevicesFDA
Biomet, Inc. recalls Knee Products: 183742 Vanguard Knee System, PS+ Tibial Bearing, 12 MM, 71/75 MM EP-183608 Vanguard Knee Syst
Hazard: Potential presence of elevated endotoxin levels that exceed the specification limit
June 3, 2020Medical DevicesFDA
Biomet, Inc. recalls Knee Products: 189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM 189422 Vanguard Knee System, PS
Hazard: Potential presence of elevated endotoxin levels that exceed the specification limit