GLOBAL AP 2130-01-030Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL AP BROACH / IMPLANT HANDLE · Class 1
All models of GLOBAL AP (40)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295090519), received between Mar 6, 2018 and Jun 22, 2022 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Most reported problems
Device problems
- Break2
- Dull, Blunt1
- Material Deformation1
- Unintended Movement1
Patient problems
- No Consequences Or Impact To Patient3
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 22, 2022Unintended Movement; Unintended Movement
IT WAS REPORTED THAT THE BROACH HANDLE WAS LOOSE WHEN SURGEON WAS BROACHING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14775540 ↗MalfunctionFeb 18, 2020Break; Break
IT WAS REPORTED THAT THE ROCKER BAR BROKE INTO TWO PIECES. 3 PIECES ALL TOGETHER. ALL PIECES RECOVERED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9718895 ↗MalfunctionFeb 21, 2019Dull, Blunt; Material Deformation; Dull, Blunt; Material Deformation
UPON INSPECTION OF INSTRUMENT TRAYS PRIOR TO THEM BEING DELIVERED TO A CUSTOMER FOR AN UPCOMING CASE, REP NOTICE METAL BURRS AND SPIKES ON HUMERAL BROACH HANDLE THAT WOULD HAVE RESULTED IN A COMPROMISE TO STERILITY AND POSSIBLE INJURY TO SURGEON CUSTOMER.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8359372 ↗MalfunctionMar 6, 2018Break; Break
TOTAL SHOULDER JOINT REPLACEMENT (B)(6), (B)(6) HOSPITAL, (B)(6) 2018. THE SURGEON WAS HAMMERING THE BROACH INTO THE HUMERUS AND THE SMALL METAL TOGGLE BROKE IN HALF AND FELL OFF. BROKEN PIECES ISOLATED AND REMOVED FROM STERILE FIELD. THE SURGEON WAS ABLE TO CARRY ON WITHOUT ISSUE. NO AE TO PATIENT. NO DELAY TO PROCEDURE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7317576 ↗
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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