BIRMINGHAM HIP RESURFACING (BHR)Recalls & reported problems across all models
Smith & Nephew, Inc. · 47 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,300
- Deaths reported
- 8
- Injuries reported
- 1,270
- Recalls
- 0
We found 47 models of BIRMINGHAM HIP RESURFACING (BHR) by Smith & Nephew, Inc. in the FDA's device registry (GUDID). Together they are named in 1,300 adverse event reports in the FDA's MAUDE database, received between Mar 30, 2016 and Jul 1, 2026 — classified as 8 deaths, 1,270 injuries, 22 malfunctions.
The most frequently reported specific device problem is “Biocompatibility” (508 reports).
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
Most reported BIRMINGHAM HIP RESURFACING (BHR) problems
Device problems
- Adverse Event Without Identified Device or Use Problem510
- Biocompatibility508
- Appropriate Device Problem Term/Code Not Available202
- Insufficient Device Problem Information158
- Patient Device Interaction Problem118
- Loosening of Implant Not Related to Bone-Ingrowth41
- Fracture39
- Patient-Device Incompatibility26
Patient problems
- Metal Related Pathology522
- Pain460
- Failure of Implant277
- Injury205
- Toxicity171
- No Code Available122
- Test Result98
- High metal ion levels95
BIRMINGHAM HIP RESURFACING (BHR) models
47 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BIRMINGHAM HIP RESURFACING (BHR) 74120156Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing3 deaths145 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120152Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing139 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74121146Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing91 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74121150Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 death86 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122154Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing75 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120154Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing2 deaths70 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122158Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing69 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120160Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing62 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120158Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing60 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120150Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing58 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74121142Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 death57 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120148Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 death56 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74123148Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing54 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122150Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing43 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74121154Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing42 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74123152Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing37 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74123144Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing28 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122152Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing13 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122160Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing13 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120162Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing11 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120146Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing9 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122162Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing8 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74123140Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing8 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122156Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing7 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122146Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing7 reports
- BIRMINGHAM HIP RESURFACING (BHR) 90128275Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing7 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120144Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing6 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74121138Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing6 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74123156Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing6 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74121158Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing4 reports
- BIRMINGHAM HIP RESURFACING (BHR) 90127585Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing3 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120164Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing2 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74120246Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing2 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122148Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing2 reports
- BIRMINGHAM HIP RESURFACING (BHR) 74122256Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing2 reports
- BIRMINGHAM HIP RESURFACING (BHR) 90127736Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 74120166Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 74120250Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 74120254Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 74120258Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 74120266Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 90128255Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 74122164Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING (BHR) 90129412Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
- BIRMINGHAM HIP RESURFACING(BHR) 90035582ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- BIRMINGHAM HIP RESURFACING(BHR) 90035583ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- BIRMINGHAM HIP RESURFACING (BHR) 90127580Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing1 report
Recent BIRMINGHAM HIP RESURFACING (BHR) adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJul 1, 2026Biocompatibility
IT WAS REPORTED THAT, AFTER UNDERWENT A BHR IN 2016, PATIENT EXPERIENCED HEAVY METAL POISONING OF THE BODY ALONG WITH PAIN. THIS ADVERSE EVENT WAS ADDRESSED BY PERFORMING A REVISION SURGERY ON (B)(6) 2026, DURING WHICH THE FEMORAL HEAD 48MM & ACETABULAR CUP HAP SIZE 48/54 WERE EXCHANGED. PATIENT'S CURRENT CONDITION IS UNKNOWN.
Patient problems: High metal ion levels; Pain
MAUDE report 25681015 ↗InjuryJun 9, 2026Biocompatibility
IT WAS REPORTED THAT, AFTER THE PLAINTIFF UNDERWENT A LEFT BHR-THA SURGERY ON (B)(6) 2010 DUE TO BILATERAL OSTEOARTHRITIS, SHE EXPERIENCED PAIN AND THIS WAS INTERFERING WITH HER DAILY ACTIVITIES. A DECREASED RANGE OF MOTION WAS NOTICED AS WELL. IT WAS DETERMINED THAT THE METAL-ON-METAL ARTICULATION WITH ASR CUP IMPLANTED HAD FAILED. THIS ADVERSE EVENT WAS ADDRESSED BY PERFORMING A REVISION SURGERY ON (B)(6) 2025, DURING WHICH SURGEON CONVERTED TO TOTAL HIP REPLACEMENT ARTHROPLASTY. THERE WERE METAL DEBRIS PRESENT ON THE INSIDE OF THE FEMORAL HEAD AND THE TRUNNION. THERE WAS APPROXIMATELY 30% ABDUCTOR DAMAGE AS A DIRECT RESULT OF METALLOSIS DAMAGE TO THE ABDUCTOR MUSCLES. THE STEM WAS STABLE AND WELL FIXED, SO IT WAS NOT REVISED. THE SURGEON NOTICED METALLOSIS STAINED TISSUE THROUGHOUT THE HIP JOINT, MOST PRONOUNCED ANTERIOR HIP CAPSULE AND SURROUNDING THE PROXIMAL FEMORAL STEM. IT WAS ALSO EXTENSIVE ALONG THE POSTERIOR CAPSULE AND SOFT TISSUES OF PROXIMAL FEMUR; AND ALONG THE BACKSIDE OF THE ACETABULAR IMPLANT. THE CUP WAS EASILY REMOVED, THE HEAD WAS NOTICED TO HAVE METAL DEBRIS INSIDE THE TRUNNION AREA, THIS WAS REMOVED AND REPLACED. THE STEM TRUNNION ALSO HAD METAL DEBRIS BUT WA
Patient problems: Loss of Range of Motion; Metal Related Pathology; Pain
MAUDE report 25439193 ↗InjuryJun 4, 2026Biocompatibility
IT WAS REPORTED THAT, AFTER UNDERWENT A BHR-LEFT HIP ON (B)(6) 2004 & A BHR-RIGHT HIP (B)(6) 2006 DUE TO UNKNOWN REASONS. THERE WAS AN ATTEMPTED TO DO A LEFT HIP REPLACEMENT SURGERY ON (B)(6) 2016, HOWEVER, A RAPID DROP IN BLOOD PRESSURE, LED TO ABANDONMENT OF THE PROCEDURE AT THAT DATE. THEY NOTED HIS RECORDED PROBNP LEVEL WAS 235 NG/L, TO WHICH ELEVATED LEVELS WERE A KNOWN ASSOCIATION WITH COBALT-INDUCED CARDIOMYOPATHY. THE PROCEDURE WAS LATER PERFORMED ON (B)(6) 2016. PATIENT CURRENT HEALTH CONDITION IS UNKNOWN.
Patient problems: High metal ion levels; Low Blood Pressure/ Hypotension
MAUDE report 25396061 ↗MalfunctionMay 18, 2026Fracture
IT WAS REPORTED THAT, DURING A BHR SURGERY, WHEN THE SURGEON WAS IMPACTING THE ACETABULAR CUP INTO THE PATIENT, A WIRE OF ONE (1) ACETABULAR CUP HAP SIZE 52/58 WAS DETACHED FROM ITS CONNECTION POINT. NO FRAGMENTS FELL INSIDE THE PATIENT. THE PROCEDURE WAS RESUMED, WITHOUT ANY DELAY, USING AN EQUIVALENT S+N BACK-UP. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25211745 ↗InjuryMar 17, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AFTER A LEFT BHR PERFORMED ON (B)(6) 2008, PATIENT WAS HOSPITALIZED DUE TO CELLULITIS AROUND THE PERIOPERATIVE SITE ON (B)(6) 2008. THIS ADVERSE EVENT WAS TREATED WITH KEFLEX. NO FURTHER INFORMATION AVAILABLE.
Patient problems: Cellulitis
MAUDE report 24624250 ↗InjuryMar 15, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT, AFTER A THR SURGERY WAS PERFORMED ON AN UNSPECIFIED DATE, OSTEOLYSIS WAS OBSERVED BEHIND THE ACETABULAR CUP. THIS ADVERSE EVENT WAS TREATED BY A REVISION SURGERY ON (B)(6) 2026 IN WHICH A ACETLR CUP HAP 60MM W/ IMPTR WAS EXCHANGED FOR A ZIMMER G7 CUP. PATIENT'S CURRENT HEALTH STATUS IS RECOVERING.
Patient problems: Osteolysis
MAUDE report 24601480 ↗InjuryFeb 21, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT, AFTER A THR SURGERY HAD BEEN PERFORMED IN 2012, THE PATIENT PRESENTED PAINFUL HIP. THE PAIN WAS PRESENT UNTIL THIS YEAR. THIS ADVERSE EVENT WAS SOLVED BY THR REVISION SURGERY ON (B)(6) 2026, IN WHICH THE FEMORAL HEAD 48MM WAS REMOVED. THE ACETLR CUP HAP 48MM W/ IMPTR WAS MAINTAINED. PERFORMED A THA SURGERY WITH A BDMH HEAD TO MATCH THE 54-CUP. PATIENT'S CURRENT HEALTH STATUS IS UNKNOWN. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: Implant Pain
MAUDE report 24410370 ↗InjuryDec 19, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
IT WAS REPORTED THAT, DURING A BHR SURGERY PERFORMED TO THE PLAINTIFF ON (B)(6) 2011 IT WAS NOTICED THAT THE PATIENT HAD EXTREMELY HARD ACETABULAR BONE WITH SUBCHONDRAL SCLEROSIS LAYER, BEING ALMOST 9-10MM THICK. THIS REQUIRED EXTENSIVE REAMING TO GAIN ANY BLEEDING BED. AFTER THIS, THE PATIENT EXPERIENCED A PROGRESSIVE PAIN AND A LARGE CYST WAS NOTICED IN AN MRI ON (B)(6) 2024. A REVISION SURGERY WAS PERFORMED ON (B)(6) 2024 DUE TO A LOOSE FEMORAL COMPONENT AND THE PAIN MENTIONED. THE ACETABULAR COMPONENT AND FEMORAL HEAD WERE EXPLANTED AND REPLACED WITH S+N IMPLANTS (9 STANDARD POLARSTEM, 40MM +8 OXINIUM HEAD, 60/40 +0 DEGREE POLYETHYLENE LINER AND 60MM REDAPT REVISION ACETABULAR CUP). THE CURRENT HEALTH STATUS OF THE PATIENT IS UNKNOWN.
Patient problems: Aseptic loosening; Cyst(s); Implant Pain
MAUDE report 23849600 ↗InjuryDec 15, 2025Biocompatibility; Biocompatibility
IT WAS REPORTED THAT, AFTER A THR SURGERY PERFORMED ON (B)(6) 2015, THE PATIENT HAS EXPERIENCED HIP PAIN, INSTABILITY, WITH SURROUNDING AREA FROM APPARENT METALLOSIS. NO REVISION SURGERY AND NO ADDITIONAL TREATMENT WAS INDICATED BY THE HCP.
Patient problems: Foreign Body Reaction; Joint Laxity; Metal Related Pathology; Osteolysis; Pain
MAUDE report 23803391 ↗InjuryNov 7, 2025Biocompatibility; Biocompatibility
IT WAS REPORTED THAT, AFTER UNDERGOING A BHR ON (B)(6) 2010 DUE TO DEGENERATIVE ARTHRITIS OF THE RIGHT HIP, THE PATIENT SUFFERED FROM A FAILED RIGHT HIP RESURFACING BECAUSE SHE HAS HAD PROGRESSIVE PAIN, ELEVATED METAL IONS, AND LOOSENING OF ACETABULAR COMPONENT. THIS ADVERSE EVENT WAS ADDRESSED BY CONDUCTING A REVISION SURGERY ON (B)(6) 2025, DURING WHICH THE WHOLE HIP SYSTEM WAS EXPLANTED. DURING PROCEDURE, AN ANTERIOR CAPSULECTOMY WAS PERFORMED. UPON ENTERING THE JOINT, THERE WAS NO OBVIOUS INFECTION OR PURULENCE. THE FINAL FEMORAL COMPONENT WAS NOW IMPACTED, USING GREAT CARE TO EVALUATE THE CALCAR, WHICH REMAINED STABLE DURING IMPACTION, NO VISUAL DEFECTS OCCURRED; FLUOROSCOPIC IMAGES CONFIRMED THIS. THE PATIENT WAS AWOKEN AND SENT TO THE POST-ANESTHESIA CARE UNIT IN STABLE CONDITION.
Patient problems: Abnormal scarring; High metal ion levels; Joint Laxity; Pain
MAUDE report 23501105 ↗InjuryNov 4, 2025Biocompatibility; Biocompatibility
IT WAS REPORTED THAT AFTER UNDERGOING A BHR ON (B)(6) 2012 DUE TO DEGENERATIVE ARTHRITIS OF THE LEFT HIP, THE PATIENT EXPERIENCED A FAILED LEFT HIP RESURFACING CHARACTERIZED BY PROGRESSIVE PAIN, ELEVATED METAL ION LEVELS, AND LOOSENING OF THE ACETABULAR COMPONENT. THE ADVERSE EVENT WAS ADDRESSED WITH A REVISION SURGERY ON 2025, DURING WHICH THE ENTIRE HIP SYSTEM WAS EXPLANTED. DURING THE PROCEDURE, AN ANTERIOR CAPSULECTOMY WAS PERFORMED, AND UPON ENTERING THE JOINT, NO SIGNS OF INFECTION OR PURULENCE WERE OBSERVED. THE FINAL FEMORAL COMPONENT WAS IMPACTED WITH GREAT CARE TO EVALUATE THE CALCAR, WHICH REMAINED STABLE DURING IMPACTION, WITH NO VISUAL DEFECTS NOTED; FLUOROSCOPIC IMAGES CONFIRMED STABILITY. THE PATIENT WAS AWAKENED AND TRANSFERRED TO THE POST-ANESTHESIA CARE UNIT IN STABLE CONDITION.
Patient problems: Deformity/ Disfigurement; High metal ion levels; Pain
MAUDE report 23461624 ↗InjuryOct 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT, AFTER A BHR SURGERY, THAT HAD BEEN PERFORMED IN 2017, THE PATIENT WAS UNHAPPY AND HAD AN ADDUCTOR REPAIR AT SOME POINT. X-RAYS SHOWED A REDUCTION IN LEG LENGTH AND OFFSET. THIS ADVERSE EVENT WAS TREATED BY A REVISION SURGERY ON (B)(6) 2025. INTRAOPERATIVELY, A NOTICEABLE NOTCHING OF THE FEMORAL NECK WAS OBSERVED. THE HEAD WAS CUT AND A HIP STEM WITH BDMH WERE IMPLANTED. THE PATIENT IS CURRENTLY WELL.
Patient problems: Bone Notching; Unequal Limb Length
MAUDE report 23438558 ↗InjuryOct 27, 2025Biocompatibility; Biocompatibility
IT WAS REPORTED THAT, ON A CLINICAL STUDY, AFTER A BHR SURGERY WAS PERFORMED ON (B)(6) 2006, ON (B)(6) 2011 THE PATIENT EXPERIENCED ATRIAL FIBRILLATION DUE TO ELEVATED ION LEVELS. IT IS UNKNOWN HOW THE PATIENT WAS TREATED BACK THEN. AFTER THIS, THE PATIENT EXPERIENCED AGAIN A PAROXYSMAL ATRIAL FIBRILLATION AND UNDERWENT ELECTRICAL CARDIOVERSION ON (B)(6) 2015. PATIENT HAD 2 EPISODES OF RECURRENT ATRIAL FIBRILLATION, 1 OF THEM LASTED 24 HOURS AND THEN IT WAS REVERTED BACK TO NORMAL. THE CURRENT HEALTH STATUS OF THE PATIENT IS UNKNOWN.
Patient problems: Atrial Fibrillation; High metal ion levels
MAUDE report 23398612 ↗InjuryOct 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT, AFTER A TOTAL LEFT HIP REPLACEMENT SURGERY PERFORMED ON AN UNSPECIFIED DATE, THE PATIENT EXPERIENCED A PERI-PROSTHETIC ACETABULAR FRACTURE. THIS ADVERSE EVENT WAS ADDRESSED BY A REVISION SURGERY ON (B)(6) 2025 IN WHICH ONE (1) ACETLR CUP HAP 62MM W/ IMPTR AND ONE (1) MODULAR HEAD 54MM {} -4 (SHORT) WERE EXPLANTED. A COMPETITOR REVISION CUP AND AN S+N FEMORAL HEAD WERE PLACED. ONE (1) SYN POR PLUS HA SO STEM SZ 18 WAS RETAINED IN-SITU. THE CURRENT HEALTH STATUS OF THE PATIENT IS UNKNOWN.
Patient problems: Periprosthetic fracture
MAUDE report 23289612 ↗InjuryOct 15, 2025Biocompatibility; Biocompatibility
IT WAS REPORTED THAT, AFTER THE PLAINTIFF UNDERWENT A LEFT BHR ON (B)(6) 2013 DUE TO OSTEOARTHRITIS, THE PATIENT STARTED TO EXPERIENCE PAIN AND WAS WORSE WHEN HE FIRST GOT UP. THE PATIENT IS A BILATERAL BHR PATIENT. LAB TESTS REVEALED ELEVATED COBALT AND CHROMIUM IONS LEVELS. THE RIGHT HIP WAS REVISED ON 25-JUL-2024 ((B)(4)), WHERE HE WAS DIAGNOSED WITH METALLOSIS, BUT THE LEFT HIP HASN¿T BEEN REVISED AT THE TIME. THE CURRENT HEALTH STATUS OF THE PATIENT IS UNKNOWN.
Patient problems: Metal Related Pathology; No Clinical Signs, Symptoms or Conditions
MAUDE report 23288042 ↗
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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.
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