ENDURANCE 2521-03-510Recalls & reported problems
Depuy Orthopaedics, Inc. · ENDURANCE BROACH SIZE 3 · Class 1
All models of ENDURANCE (20)
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 10603295127925), received between Aug 10, 2018 and Aug 28, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).
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 Available1
- Device-Device Incompatibility1
- Failure to Cut1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Not Applicable1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE SZ 1 REPLACEMENT BROACHES ARRIVED AND WERE A DIFFERENT DESIGN. NECK SEGMENTS WERE TOO LOOSE ON THE NEW BROACHES. UNKNOWN SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17634501 ↗MalfunctionDec 2, 2020Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE BROACHES ARE DULL AND NEED REPLACING. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10931346 ↗MalfunctionAug 10, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE SURGEON SUSPECTS THAT THE BROACH IS THE INCORRECT SIZE. THE MOLD DID NOT FIT DOWN THE CANAL.
Patient problems: Not Applicable
MAUDE report 7772371 ↗
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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