CORAIL L20414Recalls & reported problems
Depuy (Ireland) · CORAIL AMT BROACH 14 · Class 1
Quick summary
This DePuy CORAIL AMT broach is a surgical broach used in hip replacement. The 41 adverse event reports that name it all describe malfunctions, with no deaths or injuries. Reports mention parts breaking, deforming, or seizing together during procedures, sometimes damaging the implant. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 41
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 41 adverse event reports that list this exact device (DI 10603295258162), received between Sep 22, 2017 and Aug 3, 2026 — classified as 41 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (22 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility22
- Material Deformation5
- Material Integrity Problem4
- Break3
- Scratched Material3
- Appropriate Device Problem Term/Code Not Available2
- Contamination /Decontamination Problem2
- Difficult to Remove2
Patient problems
- No Clinical Signs, Symptoms or Conditions21
- No Consequences Or Impact To Patient14
- Insufficient Information5
- No Information1
- No Known Impact Or Consequence To Patient1
- Not Applicable1
Recent adverse event reports
The 25 most recent of 41 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 3, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50118112 ↗MalfunctionDec 4, 2025Device-Device Incompatibility; Unintended Movement; Device-Device Incompatibility; Unintended Movement
IT WAS REPORTED THAT THE NECK SEGMENT AND BROACH HANDLE WILL NOT SEAT ON BROACH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23716193 ↗MalfunctionMay 20, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT DURING A PROCEDURE HE INSTRUMENT CORAIL AMT NECK SEG 135D STD AND BROACH CORAIL SIZE 14, GOT STUCK TOGETHER WHEN TRIALING AND CANNOT BE SEPARATED. THE INSTRUMENTS SUMMIT STANDARD IMP. INSERTER AND QUICKSET TAPER HEX SCDR RIGID HAS A WORN OUT THREADS/TIP WHICH TENDS FOR THE IMPLANT TO GET STUCK AS WELL. ANOTHER SET WAS OPENED TO USE. THERE WAS NO PATIENT CONSEQUENCE. THERE WAS NO ADDITIONAL TIME REQUIRED ONLY WAS WHEN OPENING FOR ANOTHER SET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22054862 ↗MalfunctionMay 12, 2025Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
THE INSTRUMENT WAS REPORTED FOR UNKNOWN ALLEGATION. THE EVENT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22004504 ↗MalfunctionMay 1, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT WORN TRUNNION WAS STICKING TO NECK TRIAL. THERE WAS APPROXIMATELY OF 5 MINUTES OF SURGICAL DELAY. THERE WAS NO ADVERSE CONSEQUENCE THAT AFFECTED THE PATIENT BECAUSE OF THE REPORTED EVENT.
Patient problems: Insufficient Information
MAUDE report 21943584 ↗MalfunctionOct 15, 2024Device-Device Incompatibility; Material Integrity Problem; Device-Device Incompatibility; Material Integrity Problem
IT WAS REPORTED THAT A BROACH NECK WAS DAMAGED. UNABLE TO GET NECK TRIAL ON AND OFF. THE BROACH WAS SWAPPED OUT AND NEW SET USED. THERE WAS NO SURGICAL DELAY. THE PROCEDURE WAS SUCCESSFULLY COMPLETED. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20451073 ↗MalfunctionSep 19, 2024Device-Device Incompatibility; Material Integrity Problem; Device-Device Incompatibility; Material Integrity Problem
ITEM DAMAGED, WON'T CONNECT TO BROACH HANDLE ANYMORE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20263886 ↗MalfunctionJun 6, 2024Break; Break
IT WAS REPORTED THAT NECK AND TIP OF BROACH BROKE OFF. NO PIECES WERE LEFT INSIDE THE PATIENT. IT WAS UNKNOWN, IF THERE WAS A SURGICAL DELAY.
Patient problems: Insufficient Information
MAUDE report 19481477 ↗MalfunctionFeb 19, 2024Device-Device Incompatibility; Naturally Worn; Scratched Material; Device-Device Incompatibility; Naturally Worn; Scratched Material
IT WAS REPORTED THAT DURING A CASE, THE BROACH BECAME STUCK TO THE NECK TRIAL. AFTER THE SURGERY, THE BROACH WAS INSPECTED AND FOUND TO HAVE SLIGHT SCRATCHES CAUSING THE NECKS TO BECOME STUCK. OTHER BROACHES WERE TESTED TO CONFIRM THE ORIGIN OF THE ISSUE. PATIENT DELAY APPROX. 5MINS.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 18730245 ↗MalfunctionDec 8, 2023Scratched Material; Scratched Material
ADDITIONAL INFORMATION RECEIVED FROM SALES REP STATES THAT THE LOT NUMBER WAS NO LONGER VISIBLE. BEING RETURNS BY MY OFFICE. THE SURGERY WAS SLIGHTLY DELAYED. NO COMPLICATIONS OR ADVERSE EVENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18290728 ↗MalfunctionSep 22, 2023Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THE 14 BROACH BURRED AT BROACH IN BROACH HANDLE INTERFACE. IT WOULD NOT ATTACH TO BROACH HANDLE OR NECK TRIAL .
Patient problems: Insufficient Information
MAUDE report 17798103 ↗MalfunctionSep 19, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE TRIAL NECK WAS STICKING TO BROACH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17776803 ↗MalfunctionJun 20, 2023Device-Device Incompatibility; Material Integrity Problem; Device-Device Incompatibility; Material Integrity Problem
IT WAS REPORTED THAT THE PIN BROACH WAS DEFECTIVE. IT WAS IMPOSSIBLE TO PLACE THE NECK. NO PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17162979 ↗MalfunctionJun 1, 2023Device-Device Incompatibility; Material Integrity Problem; Device-Device Incompatibility; Material Integrity Problem
IT WAS REPORTED THAT THE PRODUCT IN QUESTION WAS USED IN THE SURGERY VIA BHA. DURING THE SURGERY, INTERFERENCE OCCURRED WHEN RASPING AND CHALKER REAMING TO SIZE 14. THE SHAFT PART OF THE RASP WAS DAMAGED AND THE TRIAL NECK COULD NO LONGER BE FITTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17042944 ↗MalfunctionApr 14, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE TRIAL NECKS WILL NOT FIT ON THIS BROACH. THE SURGEON REQUESTED A NEW ONE. IT WAS UNKNOWN IF THERE WAS ANY SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16746715 ↗MalfunctionApr 14, 2023Device-Device Incompatibility; Difficult to Advance; Device-Device Incompatibility; Difficult to Advance
ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE TRUNNION WAS DAMAGED, PREVENTING NECK TRIAL FROM SEATING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16742238 ↗MalfunctionFeb 8, 2023Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THE NECK SEGMENT WAS HARD TO GET ON AND OFF PROXIMAL BROACH. NO SURGICAL DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16323599 ↗MalfunctionNov 30, 2022Failure to Cut; Device-Device Incompatibility; Failure to Cut; Device-Device Incompatibility
IT WAS REPORTED THAT THE BROACH IS DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15886711 ↗MalfunctionNov 30, 2022Failure to Cut; Device-Device Incompatibility; Failure to Cut; Device-Device Incompatibility
IT WAS REPORTED THAT THE BROACH IS DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15886342 ↗MalfunctionMay 11, 2022Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE BROACHES WERE NOT CONNECTING PROPERLY TO THE BROACH HANDLE . THIS ONLY HAPPENED WITH BROACH 13 & 14, OTHER SIZES OK. THERE WAS A TEN MINUTE SURGICAL DELAY.
Patient problems: Insufficient Information
MAUDE report 14356496 ↗MalfunctionApr 14, 2022Break; Device-Device Incompatibility; Break; Device-Device Incompatibility
IT WAS REPORTED THAT THE CORAIL BROACH HAD A HARD TIME ATTACHING TO KINCISE ADAPTER AND BROACH HANDLE. ULTIMATELY GOT STUCK ON THE BROACH ADAPTER. 15 MINUTES SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14110896 ↗MalfunctionMar 30, 2022Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
UNABLE TO CONNECT TRIAL NECK SEGMENT TO BROACH. BROACH NECK SEGMENT DAMAGED. THERE WAS A SURGICAL DELAY OF THREE MINUTES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13950759 ↗MalfunctionFeb 4, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem
PROSTHESES / INSTRUMENTS FROM THE DPS JOINTS FRANCHISE ARE SHOWING (COMING OUT) SOOT AFTER THE STERILIZATION PROCESS AND THAT THE BOXES ALSO HAVE DARK SPOTS ON THE TRAYS WHICH, ACCORDING TO THE HOSPITAL, REPRESENTS THAT THE MATERIAL IS CONTAMINATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13454521 ↗MalfunctionFeb 4, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem
PROSTHESES / INSTRUMENTS FROM THE DPS JOINTS FRANCHISE ARE SHOWING (COMING OUT) SOOT AFTER THE STERILIZATION PROCESS AND THAT THE BOXES ALSO HAVE DARK SPOTS ON THE TRAYS WHICH, ACCORDING TO THE HOSPITAL, REPRESENTS THAT THE MATERIAL IS CONTAMINATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13454045 ↗MalfunctionMar 16, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE "SZ 14 CORAIL BROACH POST WOULD NOT DISENGAGE FROM THE KINCISE BROACH ADAPTER ¿1010-01-102/JJAH04185." NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11497337 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.