Compress DeviceRecalls & reported problems across all models
Biomet Orthopedics, LLC · 71 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
19 open recalls name at least one Compress Device model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 99
- Deaths reported
- 0
- Injuries reported
- 85
- Recalls
- 22
We found 71 models of Compress Device by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). Together they are named in 99 adverse event reports in the FDA's MAUDE database, received between Mar 22, 2019 and Sep 16, 2026 — classified as 85 injuries, 14 malfunctions.
The most frequently reported specific device problem is “Fracture” (44 reports).
22 FDA recall records name at least one of these models by its device identifier, 19 still open.
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
Compress Device 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.
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0388-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0387-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0386-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0385-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0384-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0383-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0382-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0381-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0380-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0379-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0378-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0377-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0376-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0375-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0374-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0373-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0372-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0371-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Oct 9, 2023Open, Classified
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
Z-0370-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Aug 21, 2019Terminated
Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
Z-0527-2020 · Root cause: Environmental control · Recall details · FDA record ↗
- Aug 21, 2019Terminated
Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
Z-0519-2020 · Root cause: Environmental control · names 39 of these models · Recall details · FDA record ↗
- Oct 24, 2018Terminated
Potential metal burrs in the holes of the device preventing the appropriate drill and transverse pins from being inserted
Z-0553-2019 · Root cause: Employee error · Recall details · FDA record ↗
Most reported Compress Device problems
Device problems
- Fracture44
- Adverse Event Without Identified Device or Use Problem25
- Migration10
- Loosening of Implant Not Related to Bone-Ingrowth9
- Detachment of Device or Device Component8
- Insufficient Device Problem Information8
- Noise, Audible3
- Difficult to Insert2
Patient problems
- Insufficient Information25
- Failure of Implant24
- Pain22
- No Clinical Signs, Symptoms or Conditions14
- Bone Fracture(s)12
- Joint Contracture9
- Loss of Range of Motion9
- No Code Available7
Compress Device models
71 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Compress® Device 178562PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls2 reports
- Compress® Device 178754shoulder prosthesis, reverse configuration2 recalls0 reports
- Compress® Device 178552Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall9 reports
- Compress® Device 178366Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall6 reports
- Compress® Device 178404Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall5 reports
- Compress® Device 178554Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall5 reports
- Compress® Device 178354Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall5 reports
- Compress® Device 178556Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall4 reports
- Compress® Device 178558PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall4 reports
- Compress® Device 178406Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall3 reports
- Compress® Device 178367PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall3 reports
- Compress® Device 178364Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall3 reports
- Compress® Device 178400PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall2 reports
- Compress® Device 178402PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall2 reports
- Compress® Device 178363Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall2 reports
- Compress® Device 178370Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall2 reports
- Compress® Device 178560PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall1 report
- Compress® Device 178362Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall1 report
- Compress® Device 178358Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall1 report
- Compress® Device 178365Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall1 report
- Compress® Device 178353Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall1 report
- Compress® Device 178355Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall1 report
- Compress® Device 178408Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall0 reports
- Compress® Device 178410Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall0 reports
- Compress® Device 178412PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall0 reports
- Compress® Device 178414Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall0 reports
- COMPRESS DEVICE 178504Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- COMPRESS DEVICE 178472Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall0 reports
- Compress® Device 178568Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall0 reports
- Compress® Device 178564Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall0 reports
- Compress® Device 178566PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- Compress® Device 178570Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- COMPRESS DEVICE 178580Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall0 reports
- COMPRESS DEVICE 178577Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall0 reports
- COMPRESS DEVICE 178730PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- COMPRESS DEVICE 178732Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall0 reports
- Compress® Device 178372Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- Compress® Device 178352Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- Compress® Device 178351PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- Compress® Device 178357Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- Compress® Device 178359Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall0 reports
- Compress® Device 178371PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 recall0 reports
- Compress® Device 178369Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 recall0 reports
- Compress® Device 178361PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall0 reports
- Compress® Device 178350Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented1 recall0 reports
- Compress® Device 178360Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- Compress® Device 178356PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 recall0 reports
- Compress® Device 178368Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- Compress® Device 178373Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 recall0 reports
- COMPRESS DEVICE 178565Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall0 reports
- COMPRESS DEVICE 178754PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall0 reports
- COMPRESS DEVICE 178759PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall0 reports
- COMPRESS DEVICE 178784PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall0 reports
- COMPRESS DEVICE 178785PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall0 reports
- COMPRESS DEVICE 178786PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall0 reports
- COMPRESS DEVICE 178787PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED1 recall0 reports
- COMPRESS DEVICE 178788PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall0 reports
- COMPRESS DEVICE 178789PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall0 reports
- Compress Device 178512PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER8 reports
- Compress® Device 178711Prosthesis, hip, constrained, cemented or uncemented, metal/polymer8 reports
- Compress® Device 178528PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED6 reports
- Compress® Device 178525PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- Compress® Device 178526Prosthesis, hip, semi-constrained, metal/polymer, cemented2 reports
- Compress® Device 178527Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented2 reports
- Compress® Device 178529Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate1 report
- Compress® Device 178535PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Compress® Device 178536Prosthesis, hip, semi-constrained, metal/polymer, cemented1 report
- Compress® Device 178538Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 report
- Compress® Device 178540Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Compress® Device 178542Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- Compress® Device 178544PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
Recent Compress Device adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Fracture
Patient problems: Foreign Body In Patient
MAUDE report 50793046 ↗MalfunctionSep 16, 2026Fracture
Patient problems: Foreign Body In Patient
MAUDE report 50793028 ↗InjuryMar 26, 2026Fracture
IT WAS REPORTED PATIENT UNDERWENT A REVISION PROCEDURE DUE TO IMPLANT FRACTURE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 24698768 ↗InjuryMar 3, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT APPROXIMATELY 9 MONTHS POST IMPLANTATION OF A COMPRESS SYSTEM, THE PATIENT EXPERIENCED SUDDEN ONSET PAIN. X-RAYS REVEALED THAT THE ANCHOR PLUG HAD FRACTURED AND SPINDLE DISASSEMBLED. SUBSEQUENTLY, THE PATIENT WAS REVISED OF THE COMPRESS SYSTEM WITH A NEW COMPRESS SYSTEM. IT IS NOTED BY THE REPORTING HEALTHCARE PROFESSIONAL THAT THE PATIENT DOES HAVE A HIGH BMI THAT MAY HAVE BEEN A CONTRIBUTING CAUSE TO THE EVENT. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: Pain
MAUDE report 24503169 ↗InjuryOct 27, 2025Fracture; Fracture
InjurySep 9, 2025Migration; Migration
IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT COMPLAINED OF PAIN OVER A SPAN OF THE LAST YEAR. THE SURGEON BELIEVED THE EXPANDABLE COMPONENT WAS EXPANDING ON ITS OWN, WITHOUT THE REQUIRED SURGERY TO EXPAND IT. THE PATIENT FELT A POP AND COULD NOT BEAR WEAR. THE PATIENT WAS THEN REVISED APPROXIMATELY 3 YEARS POST IMPLANTATION DUE TO A BROKEN ANCHOR PLUG AND THE SPINDLE LOST BONE IN-GROWTH AT THE BONE INTERFACE AND WAS NO LONGER FIXED.
Patient problems: Ambulation or Postural Difficulties; Pain
MAUDE report 23010335 ↗InjurySep 9, 2025Migration; Migration
IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT COMPLAINED OF PAIN OVER A SPAN OF THE LAST YEAR. THE SURGEON BELIEVED THE EXPANDABLE COMPONENT WAS EXPANDING ON ITS OWN, WITHOUT THE REQUIRED SURGERY TO EXPAND IT. THE PATIENT FELT A POP AND COULD NOT BEAR WEAR. THE PATIENT WAS THEN REVISED APPROXIMATELY 3 YEARS POST IMPLANTATION DUE TO A BROKEN ANCHOR PLUG AND THE SPINDLE LOST BONE IN-GROWTH AT THE BONE INTERFACE AND WAS NO LONGER FIXED.
Patient problems: Ambulation or Postural Difficulties; Pain
MAUDE report 23010320 ↗InjurySep 9, 2025Migration; Migration
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Ambulation or Postural Difficulties; Pain
MAUDE report 23010307 ↗InjurySep 3, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Aseptic loosening; Pain
MAUDE report 22954786 ↗InjurySep 3, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Aseptic loosening; Pain
MAUDE report 22954772 ↗InjurySep 3, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Aseptic loosening; Pain
MAUDE report 22954641 ↗InjurySep 3, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Aseptic loosening; Pain
MAUDE report 22954531 ↗InjuryAug 12, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Bone Fracture(s); Failure of Implant
MAUDE report 22781280 ↗InjuryJun 11, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL SURGERY ON AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO THE COMPRESS SEGMENT TAPER SEPARATING. IT WAS NOTED THAT THE TECHNIQUE SAYS SCREWS ARE OPTIONAL. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: Failure of Implant
MAUDE report 22183562 ↗InjuryApr 24, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY ONE YEAR AND THREE MONTHS POST IMPLANTATION DUE TO UNKNOWN REASONS. ABNORMAL ROTATION OF THE FEMUR (EXTERNAL ROTATION AND NOT RETURN) OCCURRED WHEN THE PATIENT FELL. THE CAUSE OF THE PATIENT'S FALL IS UNKNOWN. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: Insufficient Information
MAUDE report 21901699 ↗
Other Biomet Orthopedics, LLC products
- AFFIXUSHIP FRACTURE NAIL - RIGHT39 models · 6 reports · 37 recalls
- AFFIXUSHIP FRACTURE NAIL - LEFT27 models · 7 reports · 24 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
- Comprehensive Shoulder System68 models · 191 reports · 11 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