G7® Acetabular System 110010262Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
All models of G7 Acetabular System (42)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00887868356001), received between Aug 24, 2020 and Aug 26, 2024 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Migration” (2 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Migration2
- Detachment of Device or Device Component1
- Difficult to Insert1
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Failure of Implant1
- Joint Dislocation1
- No Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 26, 2024Difficult to Insert; Difficult to Insert
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20065094 ↗InjuryMay 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 19380361 ↗InjuryMay 9, 2024Migration; Migration
IT WAS REPORTED THE PATIENT HAD A SEVERE ACETABULAR DEFECT AND THE PLAN WAS TO USE AN ACETABULAR AUGMENT TO SUPPORT THE SHELL. DURING POSITIONING OF THE DEFINITIVE TM AUGMENT, IT WAS PULLED OUT OF THE WOUND AND DROPPED ON THE FLOOR, DEEMING IT UNUSABLE. NO OTHER AUGMENTS FROM THE INVENTORY AVAILABLE WERE SUITABLE FOR THE DEFECT. AS SUCH, THE SURGEON IMPLANTED THE CUP WITHOUT AN AUGMENT. INITIAL STABILITY WAS SUITABLE, AND THE PATIENT WAS CLOSE. THE FOLLOWING DAY, THE PATIENT DISLOCATED. IT WAS FOUND THAT THE CUP HAD SUBSIDED AND DISLOCATED. THE PATIENT WAS BROUGHT BACK TO THEATRE TO REMOVE THE CUP AND REPLACE IT WITH A LARGER SIZE.
Patient problems: Joint Dislocation
MAUDE report 19282016 ↗MalfunctionJun 7, 2023Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT THERE WAS A DEBRIS (LIKE A HAIR) IN THE STERILE PACKAGE. THE PRODUCT WAS NOT USED. THERE WAS NO PATIENT INVOLVEMENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17080829 ↗MalfunctionAug 24, 2020Migration; Migration
IT WAS REPORTED A PATIENT UNDERWENT REVISION SURGERY DUE TO FREQUENT DISLOCATIONS. AFTER THE SURGERY, THE RADIOGRAPH SHOWED ONE OF THE SCREWS HAD PENETRATED THE SHELL. NO REVISION HAS BEEN REPORTED TO DUE THIS EVENT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Information
MAUDE report 10441961 ↗
Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall11 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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