Hybrid GlenoidRecalls & reported problems across all models
Biomet Orthopedics, LLC · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 51
- Deaths reported
- 0
- Injuries reported
- 51
- Recalls
- 2
We found 4 models of Hybrid Glenoid by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). Together they are named in 51 adverse event reports in the FDA's MAUDE database, received between Nov 11, 2019 and Sep 29, 2026 — classified as 51 injuries.
The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (13 reports).
2 FDA recall records 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
Hybrid Glenoid 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-2144-2020 · Root cause: Process control · Recall details · FDA record ↗
- Apr 26, 2017Terminated
Zimmer Biomet is conducting a voluntary recall for a single lot of the Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System after it was determined that two pieces from the lot were moved to finished goods and shipped despite having an open Non-Conformance Report (NCR). The NCR indicated that one piece from the lot had scratches and the other non-confirming threads.
Z-2216-2017 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported Hybrid Glenoid problems
Device problems
- Adverse Event Without Identified Device or Use Problem23
- Loosening of Implant Not Related to Bone-Ingrowth13
- Fracture8
- Device Dislodged or Dislocated6
- Naturally Worn6
- Unstable5
- Insufficient Device Problem Information4
- Detachment of Device or Device Component3
Patient problems
- Failure of Implant23
- Pain22
- Loss of Range of Motion10
- Muscle/Tendon Damage8
- Insufficient Information6
- Joint Dislocation6
- Scar Tissue4
- Subluxation4
Hybrid Glenoid models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Hybrid Glenoid 113954PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall13 reports
- Hybrid Glenoid 113956PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED1 recall2 reports
- Hybrid Glenoid PT-113950PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED22 reports
- Hybrid Glenoid 113952PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED14 reports
Recent Hybrid Glenoid adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 29, 2026Fracture; Loosening of Implant Not Related to Bone-Ingrowth
Patient problems: Joint Impingement
MAUDE report 50933799 ↗InjuryNov 26, 2025Failure to Osseointegrate; Failure to Osseointegrate
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Medical device site infection; Pain
MAUDE report 23660159 ↗InjuryNov 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL SHOULDER PROCEDURE AND WAS SUBSEQUENTLY REVISED AFTER A ROTATOR CUFF FAILURE DUE TO A FALL. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Insufficient Information; Muscle/Tendon Damage
MAUDE report 23468394 ↗InjuryNov 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL SHOULDER PROCEDURE AND WAS SUBSEQUENTLY REVISED AFTER A ROTATOR CUFF FAILURE DUE TO A FALL. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Insufficient Information; Muscle/Tendon Damage
MAUDE report 23468391 ↗InjuryMar 24, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE PATIENT UNDERWENT A SHOULDER REVISION APPROXIMATELY SEVEN (7) YEARS AND NINE (9) MONTHS POST-IMPLANTATION DUE TO A ROTATOR CUFF TEAR. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Muscle/Tendon Damage
MAUDE report 21677623 ↗InjuryNov 25, 2024Fracture; Naturally Worn; Loosening of Implant Not Related to Bone-Ingrowth; Fracture; Naturally Worn; Loosening of Implant Not Related to Bone-Ingrowth
NO ADDITIONAL INFORMATION IS AVAILABLE REGARDING THE INCIDENT.
Patient problems: Bone Fracture(s); Failure of Implant; Metal Related Pathology; Pain
MAUDE report 20772548 ↗InjuryOct 17, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
NO ADDITIONAL INFORMATION IS AVAILABLE REGARDING THE INCIDENT.
Patient problems: Joint Dislocation
MAUDE report 20474182 ↗InjurySep 17, 2024Naturally Worn; Naturally Worn
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant; Pain
MAUDE report 20238076 ↗InjuryMar 21, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE INITIAL RIGHT SHOULDER ARTHROPLASTY APPROXIMATELY 9 YEARS AGO. SUBSEQUENTLY ABOUT A MONTH AGO THE PATIENT REPORTED UNUSUAL PAIN AND A DECREASE IN RANGE OF MOTION WITH REFERRAL FOR CONSULTANT AND UNKNOWN TREATMENT. ATTEMPTS HAVE BEEN MADE AND THERE IS NO FURTHER INFORMATION AT THIS TIME.
Patient problems: Connective Tissue Disease; Loss of Range of Motion; Pain
MAUDE report 18954021 ↗InjuryMar 8, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED UNDERWENT A REVISION PROCEDURE TO A REVERSE TOTAL SHOULDER FOR INSTABILITY AND TWO EVENTS OF LUXATION APPROXIMATELY TWO YEARS POST INITIAL PROCEDURE. ALL COMPONENTS, EXCEPT FOR STEM, WAS REVISED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.
Patient problems: Subluxation
MAUDE report 18866428 ↗InjuryDec 21, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18371688 ↗InjuryDec 18, 2023Fracture; Fracture
IT WAS REPORTED PATIENT WAS REVISED DUE TO ROTATOR CUFF FAILURE AND IMPLANT FRACTURE APPROXIMATELY EIGHT MONTHS POST OPERATION. THE GLENOID POST AND POLY WERE EXCHANGED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Muscle/Tendon Damage
MAUDE report 18348093 ↗InjuryNov 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL ANATOMIC SHOULDER REPLACEMENT ONE (1) YEAR AND NINE MONTHS AGO. SUBSEQUENTLY, THE PATIENT WAS REVISED DUE TO THE PATIENT'S ROTATOR CUFF FAILING. THE IMPLANT WAS EXPLANTED, AND A MINI BASEPLATE WAS IMPLANTED ALONG WITH A GLENOSPHERE, SCREWS, AND MINI HUMERAL TRAY AND BEARING.
Patient problems: Muscle/Tendon Damage
MAUDE report 18226903 ↗InjuryOct 5, 2023Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated
IT WAS REPORTED THAT THE PATIENT IS BEING INDICATED FOR AN UPCOMING REVISION PROCEDURE DUE TO SUBLUXATION/DISLOCATION. DURING THE PATIENT'S APPOINTMENT LIGAMENT LAXITY AND VOLUNTARY INSTABILITY WERE NOTED. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Joint Dislocation; Joint Laxity; Medical device site infection; Pain
MAUDE report 17876078 ↗InjuryOct 3, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE PATIENT HAD AN INITIAL LEFT SHOULDER ARTHROPLASTY APPROXIMATELY SIX (6) AND A HALF YEARS AGO. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY FIVE (5) YEARS AGO FOR AN UNKNOWN REASON. THE PATIENT WAS REVISED FROM AND ANATOMIC SHOULDER TO A REVERSE SHOULDER.
Patient problems: Insufficient Information
MAUDE report 17861417 ↗
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.
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