GLOBAL AP 2130-10-000Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP HUMERAL STEM BROACH / TRIAL 10mm · Class 1
All models of GLOBAL AP (40)
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 10603295090724), received between Oct 26, 2017 and Oct 26, 2017 — classified as 3 malfunctions.
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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available3
Patient problems
- No Information3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 26, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT THE SCRUB NURSE WAS IDENTIFYING HUMERAL STEM BROACH/TRIAL TO LOAD AND COULD NOT READ THE SIZING ON TRIAL. SURGEON SUGGESTED THESE BE REPLACED TO FACILITATE TRIALING PROCESS.
Patient problems: No Information
MAUDE report 6979874 ↗MalfunctionOct 26, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT THE SCRUB NURSE WAS IDENTIFYING HUMERAL STEM BROACH/TRIAL TO LOAD AND COULD NOT READ THE SIZING ON TRIAL. SURGEON SUGGESTED THESE BE REPLACED TO FACILITATE TRIALING PROCESS.
Patient problems: No Information
MAUDE report 6979855 ↗MalfunctionOct 26, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT THE SCRUB NURSE WAS IDENTIFYING HUMERAL STEM BROACH/TRIAL TO LOAD AND COULD NOT READ THE SIZING ON TRIAL. SURGEON SUGGESTED THESE BE REPLACED TO FACILITATE TRIALING PROCESS.
Patient problems: No Information
MAUDE report 6979134 ↗
Other BROACH devices
- NA 2598-07-550Depuy (Ireland) · BROACH323 reports
- SUMMIT 2570-00-000Depuy (Ireland) · BROACH269 reports
- NA 952212500FDepuy (Ireland) · BROACH245 reports
- ACTIS 2010-01-050Depuy (Ireland) · BROACH235 reports
- CORAIL 9522-11-500Depuy (Ireland) · BROACH210 reports
- ACTIS 2010-01-060Depuy (Ireland) · BROACH186 reports
- ACTIS 2010-01-040Depuy (Ireland) · BROACH172 reports
- ACTIS 2010-01-070Depuy (Ireland) · BROACH162 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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