SUMMIT 2570-02-300Recalls & reported problems
Depuy (Ireland) · SUMMIT TAPERED REAMER SIZE 6/7 · Class 1
All models of SUMMIT (43)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy Summit tapered reamer is a surgical bone-shaping tool used with a Hudson adapter and T-handle. The 48 reports mostly describe reamers that would not connect or lock onto the adapter, dull or bent blades that stopped cutting, and normal wear, with no deaths or injuries mentioned. 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
- 48
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 48 adverse event reports that list this exact device (DI 10603295143024), received between Oct 10, 2017 and Jul 3, 2025 — classified as 48 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (21 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 Incompatibility21
- Naturally Worn14
- Failure to Cut11
- Dull, Blunt10
- Material Deformation7
- Material Twisted/Bent7
- Appropriate Device Problem Term/Code Not Available5
- Connection Problem2
Patient problems
- No Consequences Or Impact To Patient23
- No Clinical Signs, Symptoms or Conditions16
- Insufficient Information4
- Not Applicable4
- No Information1
Recent adverse event reports
The 25 most recent of 48 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 3, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE REAMER NOT CONNECTING PROPERLY. DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22393989 ↗MalfunctionOct 30, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE HOSPITAL STAFF THREW THE BIPOLAR RETAINING CLIP IN THE TRASH, THINKING THAT IT WAS A DISPOSABLE INSTRUMENT. THE SUMMIT REAMERS HAVE ALSO BECOME DULL. THIS DID NOT DELAY SURGERY. NO OTHER INFORMATION IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 20565991 ↗MalfunctionOct 30, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE HOSPITAL STAFF THREW THE BIPOLAR RETAINING CLIP IN THE TRASH, THINKING THAT IT WAS A DISPOSABLE INSTRUMENT. THE SUMMIT REAMERS HAVE ALSO BECOME DULL. THIS DID NOT DELAY SURGERY. NO OTHER INFORMATION IS AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 20565972 ↗MalfunctionOct 11, 2024Failure to Cut; Failure to Cut
IT WAS REPORTED ON (B)(6) 2024 THAT THE HOSPITAL STAFF DROPPED THE BIPOLAR RETAINING CLIP. THE SUMMIT REAMERS HAVE BECOME DULL. THIS DID NOT DELAY SURGERY.
Patient problems: Insufficient Information
MAUDE report 20429431 ↗MalfunctionJan 3, 2024Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE DEVICE WOULD NOT ENGAGE IN THE HUDSON ADAPTER. SURGICAL DELAY WAS UNKNOWN.
Patient problems: Insufficient Information
MAUDE report 18435464 ↗MalfunctionOct 20, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT ON OCT 13, 2023, THE PATIENT UNDERWENT A BHA. DURING SURGERY, THE T-HANDLE IN QUESTION AND A REAMER DID NOT MATCH, SO THE T-HANDLE IN QUESTION COULD NOT BE USED. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17974294 ↗MalfunctionSep 28, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT 6/7 REAMER WAS NO LONGER ATTACHED TO THE HUDSON ADAPTER. IT IS UNKNOWN IF THERE WAS ANY SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17837346 ↗MalfunctionJul 13, 2023Failure to Cut; Device-Device Incompatibility; Naturally Worn; Failure to Cut; Device-Device Incompatibility; Naturally Worn
IT WAS REPORTED THAT THE PROXIMAL END WILL NOT LOCK ONTO THE HUDSON ADAPTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17320241 ↗MalfunctionJul 13, 2023Failure to Cut; Device-Device Incompatibility; Naturally Worn; Failure to Cut; Device-Device Incompatibility; Naturally Worn
IT WAS REPORTED THAT THE PROXIMAL END WOULD NOT LOCK ONTO THE HUDSON ADAPTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17319451 ↗MalfunctionOct 13, 2022Break; Device-Device Incompatibility; Break; Device-Device Incompatibility
IT WAS REPORTED THAT THE CONICAL REAMER WONT ATTACH TO STRYKER POWER CHUCK. NO DELAY IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15594426 ↗MalfunctionOct 3, 2022Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE REAMER WILL NOT ATTACH TO POWER AND T-HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15528253 ↗MalfunctionMay 4, 2022Naturally Worn; Naturally Worn
INSTRUMENTS ARE WORN. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14277224 ↗MalfunctionMay 4, 2022Naturally Worn; Naturally Worn
INSTRUMENTS ARE WORN. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14277122 ↗MalfunctionMay 4, 2022Naturally Worn; Naturally Worn
INSTRUMENTS ARE WORN. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14277059 ↗MalfunctionMay 4, 2022Naturally Worn; Naturally Worn
INSTRUMENTS ARE WORN. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14276878 ↗MalfunctionMay 4, 2022Naturally Worn; Naturally Worn
INSTRUMENTS ARE WORN. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14276872 ↗MalfunctionJul 13, 2021Device-Device Incompatibility; Device-Device Incompatibility
REAMER WOULD NOT STAY ENGAGED IN THE POWER ADAPTER. WAS ABLE TO FINISH CASE WITHOUT SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12158462 ↗MalfunctionJun 11, 2021Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
REAMER UNABLE TO BE TAKEN OFF THE T HANDLE. DURING REAMING THE TEETH HAVE BENT AND NOT ENABLED THE REAMER TO COME OFF THE T HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11987868 ↗MalfunctionApr 7, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE REAMERS WILL NOT CONNECT TO HUDSON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11629826 ↗MalfunctionApr 7, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE REAMERS WILL NOT CONNECT TO HUDSON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11629825 ↗MalfunctionMar 20, 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 9859651 ↗MalfunctionMar 20, 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 9859649 ↗MalfunctionFeb 5, 2020Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE SUMMIT STRAIGHT REAMER SIZES 0-1,2-3,4-5,6-7,8-9, AND LATERALIZER ARE STRIPPED AT THE TOP AND WILL NOT WORK PROPERLY IN THE HUDSON ADAPTOR. NO PIECES ARE BROKEN AND ALL PARTS WERE RETRIEVED AND SENT TO THE OFFICE. THE SCRUB TECHNIQUE MADE ME AWARE. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9672569 ↗MalfunctionJan 10, 2020Connection Problem; Device-Device Incompatibility; Material Deformation; Material Twisted/Bent; Naturally Worn; Connection Problem; Device-Device Incompatibility; Material Deformation; Material Twisted/Bent; Naturally Worn
IT WAS REPORTED THAT THE 6/7 SUMMIT DISTAL REAMER IS WORN AT THE CONNECTION POINT AND IS NOT FUNCTIONING AS INTENDED WHERE THE TIP OF THE REAMER CONNECTS TO THE DRILL.. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9577997 ↗MalfunctionOct 31, 2019Dull, Blunt; Failure to Cut; Dull, Blunt; Failure to Cut
IT WAS REPORTED THAT THE SUMMIT SZ0/1, 2/3, 4/5, 6/7, 8/9 TAPERED REAMER ARE ALL DULL. NEEDS REPLACEMENT X'S 4.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9263371 ↗
Other REAMER devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 reports
- QUICKSET 2440-00-553Depuy (Ireland) · REAMER1,105 reports
- QUICKSET 2440-00-547Depuy (Ireland) · REAMER1,073 reports
- QUICKSET 2440-00-555Depuy (Ireland) · REAMER1,065 reports
- QUICKSET 2440-00-557Depuy (Ireland) · REAMER1,031 reports
- QUICKSET 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 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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