OSS Orthopedic Salvage SystemRecalls & reported problems across all models
Biomet Orthopedics, LLC · 76 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 181
- Deaths reported
- 0
- Injuries reported
- 171
- Recalls
- 1
We found 76 models of OSS Orthopedic Salvage System by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). Together they are named in 181 adverse event reports in the FDA's MAUDE database, received between Oct 17, 2019 and Aug 24, 2026 — classified as 171 injuries, 10 malfunctions.
The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (27 reports).
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
OSS Orthopedic Salvage System recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Apr 17, 2020Terminated
Potential presence of elevated endotoxin levels that exceed the specification limit
Z-2147-2020 · Root cause: Process control · Recall details · FDA record ↗
Most reported OSS Orthopedic Salvage System problems
Device problems
- Adverse Event Without Identified Device or Use Problem65
- Loosening of Implant Not Related to Bone-Ingrowth27
- Fracture26
- Unstable23
- Patient Device Interaction Problem17
- Detachment of Device or Device Component15
- Insufficient Device Problem Information15
- Device Dislodged or Dislocated11
Patient problems
- Failure of Implant61
- Pain58
- Insufficient Information39
- Ambulation or Postural Difficulties14
- Muscle/Tendon Damage14
- Hyperextension13
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available12
- Bacterial Infection12
OSS Orthopedic Salvage System models
76 models, most reported first. Each model has its own page with its reports, recalls and device details.
- OSS™ Orthopedic Salvage System 150414PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall3 reports
- OSS™ Orthopedic Salvage System 150476PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER14 reports
- OSS™ Orthopedic Salvage System 150477PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER11 reports
- OSS™ Orthopedic Salvage System 150410PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER10 reports
- OSS™ Orthopedic Salvage System 150478PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER10 reports
- OSS™ Orthopedic Salvage System 150480PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER9 reports
- OSS™ Orthopedic Salvage System 150354Prosthesis, hip, semi-constrained, metal/polymer, cemented6 reports
- OSS™ Orthopedic Salvage System 150461Prosthesis, hip, semi-constrained, metal/polymer, cemented6 reports
- OSS™ Orthopedic Salvage System 150355Prosthesis, hip, semi-constrained, metal/polymer, cemented5 reports
- OSS™ Orthopedic Salvage System 150412Prosthesis, hip, semi-constrained, metal/polymer, cemented4 reports
- OSS™ Orthopedic Salvage System 150415Prosthesis, hip, semi-constrained, metal/polymer, cemented4 reports
- OSS™ Orthopedic Salvage System 150411Prosthesis, hip, semi-constrained, metal/polymer, cemented4 reports
- OSS™ Orthopedic Salvage System 150457Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate4 reports
- OSS™ Orthopedic Salvage System 150510PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- OSS™ Orthopedic Salvage System 161035PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- OSS™ Orthopedic Salvage System 161094PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER4 reports
- OSS™ Orthopedic Salvage System 150356PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- OSS™ Orthopedic Salvage System 150364PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- OSS™ Orthopedic Salvage System 161073PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- OSS™ Orthopedic Salvage System 150419PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150362PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150366PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150417Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- OSS™ Orthopedic Salvage System 150425Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- OSS™ Orthopedic Salvage System 150446PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150464PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150465PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150473Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- OSS™ Orthopedic Salvage System 150482PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 161068PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 161075PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 161095PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 reports
- OSS™ Orthopedic Salvage System 150420PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System CP111649Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System CP111652Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150359PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150360Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150363PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150365Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150368Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150369Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150375Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150380Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150381Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150388Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150394PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150397PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150398Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150424PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150426Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- OSS™ Orthopedic Salvage System 150443PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150445PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150466PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150467PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150468PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150469PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150471PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 150483PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161077PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161071PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161065PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161070PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161079PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161096PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161098PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161123PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161124PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System CP113461PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System CP113836PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 151806PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OSS™ Orthopedic Salvage System 151855PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 151838PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- OSS™ Orthopedic Salvage System 151844PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System CP113462PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161034PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- OSS™ Orthopedic Salvage System 161012PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
Recent OSS Orthopedic Salvage System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 24, 2026Adverse Event Without Identified Device or Use Problem
It was reported that the patient underwent a right knee arthroplasty revision to address a femoral periprosthetic fracture after a fall approximately five (5) months post-operatively.No additional information is available.
Patient problems: Bone Fracture(s); Fall
MAUDE report 50410549 ↗InjuryAug 20, 2026Adverse Event Without Identified Device or Use Problem
It was reported that a patient was revised approximately two months post implantation due to pain after falling and fracturing the femur bone. The prosthesis is not damaged. The surgeon changed the uncemented stem to a cemented stem and increased the poly thickness. Attempts to obtain additional information have been made; however, no more information is available.
Patient problems: Bone Fracture(s); Fall; Pain
MAUDE report 50354424 ↗InjuryAug 17, 2026Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
It was reported that the patient underwent a knee arthroplasty revision of the femoral component to address unknown complications nearly four (4) months post-operatively.Attempts have been made, however, no additional information is available.
Patient problems: Insufficient Information; Medical device site infection; Pain
MAUDE report 50279823 ↗InjuryAug 3, 2026Loosening of Implant Not Related to Bone-Ingrowth
It was reported that the patient underwent a right knee arthroplasty revision to address femoral loosening approximately two (2) years post-operatively.Attempts have been made, however, no additional information is available.
Patient problems: Aseptic loosening
MAUDE report 50119228 ↗InjuryJun 17, 2026Loosening of Implant Not Related to Bone-Ingrowth
IT WAS REPORTED THAT THE PATIENT UNDERWENT A KNEE ARTHROPLASTY REVISION TO ADDRESS PAIN AND FEMORAL IMPLANT LOOSENING AFTER A FALL APPROXIMATELY TWO (2) YEARS POST-OPERATIVELY. ATTEMPTS HAVE BEEN MADE, HOWEVER, NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: Aseptic loosening; Pain
MAUDE report 25535622 ↗InjuryJun 11, 2026Fracture
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL TOTAL KNEE ARTHROPLASTY ON AN UNKNOWN DATE AND WAS SUBSEQUENTLY REVISED DUE TO A PERIPROSTHETIC FRACTURE FOLLOWING A FALL AND NEW COMPONENT WERE IMPLANTED. THE PATIENT DID WELL UNTIL DEVELOPING SLIGHT RECURVATUM WITH KNEE EXTENSION BEYOND NEUTRAL. THE PATIENT THEN UNDERWENT A POLYETHYLENE INSERT EXCHANGE, AND INTRA-OPERATIVELY THE BEARING WAS OBSERVED TO BE CRACKED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hyperextension
MAUDE report 25471043 ↗InjuryNov 14, 2025Fracture; Unstable; Patient-Device Incompatibility; Fracture; Unstable; Patient-Device Incompatibility
IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT KNEE ARTHROPLASTY REVISION TO ADDRESS EXCESSIVE HYPEREXTENSION AND INSTABILITY APPROXIMATELY ONE (1) YEAR POST-OPERATIVELY. DURING THE REVISION, THE FEMORAL BUSHINGS AND POLYETHYLENE TIBIAL BEARING WERE IDENTIFIED TO HAVE FRACTURED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hyperextension
MAUDE report 23556749 ↗InjuryNov 14, 2025Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem; Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Hyperextension
MAUDE report 23555818 ↗InjuryNov 14, 2025Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem; Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT KNEE ARTHROPLASTY REVISION TO ADDRESS EXCESSIVE HYPEREXTENSION AND INSTABILITY APPROXIMATELY ONE (1) YEAR POST-OPERATIVELY. DURING THE REVISION, THE FEMORAL BUSHINGS AND POLYETHYLENE TIBIAL BEARING WERE IDENTIFIED TO HAVE FRACTURED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hyperextension
MAUDE report 23555805 ↗InjuryNov 14, 2025Fracture; Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem; Fracture; Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT KNEE ARTHROPLASTY REVISION TO ADDRESS EXCESSIVE HYPEREXTENSION AND INSTABILITY APPROXIMATELY ONE (1) YEAR POST-OPERATIVELY. DURING THE REVISION, THE FEMORAL BUSHINGS AND POLYETHYLENE TIBIAL BEARING WERE IDENTIFIED TO HAVE FRACTURED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hyperextension
MAUDE report 23555784 ↗InjuryNov 14, 2025Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem; Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT KNEE ARTHROPLASTY REVISION TO ADDRESS EXCESSIVE HYPEREXTENSION AND INSTABILITY APPROXIMATELY ONE (1) YEAR POST-OPERATIVELY. DURING THE REVISION, THE FEMORAL BUSHINGS AND POLYETHYLENE TIBIAL BEARING WERE IDENTIFIED TO HAVE FRACTURED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hyperextension
MAUDE report 23555715 ↗InjuryNov 14, 2025Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem; Unstable; Patient-Device Incompatibility; Patient Device Interaction Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT KNEE ARTHROPLASTY REVISION TO ADDRESS EXCESSIVE HYPEREXTENSION AND INSTABILITY APPROXIMATELY ONE (1) YEAR POST-OPERATIVELY. DURING THE REVISION, THE FEMORAL BUSHINGS AND POLYETHYLENE TIBIAL BEARING WERE IDENTIFIED TO HAVE FRACTURED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hyperextension
MAUDE report 23555711 ↗InjurySep 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO STIFFNESS/ SCAR TISSUE ONE YEAR, EIGHT MONTHS POST INITIAL IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: Loss of Range of Motion; Pain; Scar Tissue
MAUDE report 22983704 ↗InjurySep 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO STIFFNESS/ SCAR TISSUE ONE YEAR, EIGHT MONTHS POST INITIAL IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: Loss of Range of Motion; Pain; Scar Tissue
MAUDE report 22983639 ↗InjurySep 5, 2025Fracture; Adverse Event Without Identified Device or Use Problem; Fracture; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO STIFFNESS/ SCAR TISSUE ONE YEAR, EIGHT MONTHS POST INITIAL IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: Failure of Implant; Loss of Range of Motion; Pain; Scar Tissue
MAUDE report 22983552 ↗
Other Biomet Orthopedics, LLC products
- AFFIXUSHIP FRACTURE NAIL - RIGHT39 models · 6 reports · 37 recalls
- AFFIXUSHIP FRACTURE NAIL - LEFT27 models · 7 reports · 24 recalls
- Compress Device71 models · 99 reports · 22 recalls
- Arcos Modular Revision Hip System71 models · 191 reports · 19 recalls
- Comprehensive Reverse Shoulder57 models · 895 reports · 3 recalls
- Vanguard Knee System147 models · 306 reports · 13 recalls
- STAGEONE17 models · 0 reports · 18 recalls
- StageOne Select15 models · 2 reports · 15 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page