SUMMIT 2570-00-165Recalls & reported problems
Depuy (Ireland) · SUMMIT BROACH SIZE 9 · Class 1
All models of SUMMIT (43)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295142966), received between Mar 23, 2020 and Feb 26, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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
- Device-Device Incompatibility2
- Dull, Blunt2
- Failure to Cut2
- Illegible Information2
- Material Twisted/Bent2
- Material Deformation1
- Material Integrity Problem1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 26, 2024Device-Device Incompatibility; Device-Device Incompatibility
ADDITIONAL INFORMATION WAS RECEIVED: A. WAS THERE A SURGICAL DELAY BECAUSE OF THIS EVENT? IF YES, WHAT IS THE DURATION OF THE DELAY? NO. B. WAS THERE ANY ADVERSE CONSEQUENCES THAT AFFECTED THE PATIENT BECAUSE OF THE REPORTED EVENT? NO.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18776963 ↗MalfunctionAug 5, 2022Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THERE IS A BURR ON THE BROACH POST AND IT WILL NOT LOCK ONTO HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15176431 ↗MalfunctionApr 21, 2021Material Integrity Problem; Mechanical Jam; Material Integrity Problem; Mechanical Jam
IT WAS REPORTED THAT THE SUMMIT SIZE 9 BROACH WAS STUCK IN THE CANAL. EXTRACTION WAS EXTREMELY DIFFICULT AND UPON REMOVAL, THE BROACH WAS DAMAGED." NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11701597 ↗MalfunctionMar 23, 2020Dull, Blunt; Failure to Cut; Material Twisted/Bent; Illegible Information; Dull, Blunt; Failure to Cut; Material Twisted/Bent; Illegible Information
SIZE ETCHINGS ARE WORN AND NOT LEGIBLE, AND EDGES ARE DULL AND NOT ADEQUATE IN CUTTING BONE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9868069 ↗MalfunctionMar 23, 2020Dull, Blunt; Failure to Cut; Material Twisted/Bent; Illegible Information; Dull, Blunt; Failure to Cut; Material Twisted/Bent; Illegible Information
SIZE ETCHINGS ARE WORN AND NOT LEGIBLE, AND EDGES ARE DULL AND NOT ADEQUATE IN CUTTING BONE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9868067 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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