G7 STRAIGHT MODULAR ACETABULAR 110003451Recalls & reported problems
Biomet Orthopedics, LLC · Class 3
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00880304546615), received between Oct 18, 2022 and Aug 4, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Damaged Thread” (1 report).
3 other recalls cover devices cleared under the same FDA submission (K121874); they may or may not involve this specific model.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Damaged Thread1
- Difficult to Insert1
- Fracture1
- Separation Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 4, 2025Damaged Thread; Damaged Thread
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22710400 ↗MalfunctionDec 19, 2023Fracture; Separation Failure; Fracture; Separation Failure
THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18358602 ↗MalfunctionOct 18, 2022Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT THE G& INSERTER STUCK OUT FROM THE THOP OF THE G7 CUP. AN ALTERNATE INSERTER WAS USED WITH NO FURTHER ISSUE. NO ADVERSE CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15626725 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K121874. One submission often covers many models, so check the product and lot details in each record.
- Z-0007-2023 · Aug 25, 2022 · Open, ClassifiedG7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in hip arthroplasty
- Z-1838-2014 · May 7, 2014 · TerminatedG7 Acetabular System Positioning Guide Post, orthopedic surgical instrument for hip prosthesis. PN:110003500.
- Z-1837-2014 · May 7, 2014 · TerminatedG7 Acetabular System Positioning Guide Rod, orthopedic surgical instrument for hip prosthesis PN 110003458.
Other TISSUE GRAFT OF LESS THAN 6MM devices
- G7® 010002749Biomet Orthopedics, LLC · TISSUE GRAFT OF LESS THAN 6MM2 reports
- G7 LATERAL POSITIONING GUIDE 110003456Biomet Orthopedics, LLC · TISSUE GRAFT OF LESS THAN 6MM1 report
- G7 SUPINE POSITIONING GUIDE 110003455Biomet Orthopedics, LLC · TISSUE GRAFT OF LESS THAN 6MM1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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