DELTA XTEND 2307-89-000Recalls & reported problems
Depuy (Ireland) · DELTA Xtend GLENOID CANNULATED STOP DRILL DIA 7.5MM · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy Delta Xtend cannulated stop drill is used in shoulder surgery to prepare a hole for a joint implant. The 68 reports mostly describe the drill being dull or failing to cut, sometimes leaving it stuck on the surgical wire or unable to detach from the power tool, with a few cases of bending or breaking; most procedures were completed without harm to the patient. There are no deaths and no injuries, and 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
- 68
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 68 adverse event reports that list this exact device (DI 10603295116509), received between Dec 20, 2017 and May 7, 2026 — classified as 68 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (38 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.
Reports received per month
Most reported problems
Device problems
- Failure to Cut38
- Dull, Blunt19
- Device-Device Incompatibility6
- Break2
- Material Twisted/Bent2
- Naturally Worn2
- Appropriate Device Problem Term/Code Not Available1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions40
- No Consequences Or Impact To Patient23
- Insufficient Information5
Recent adverse event reports
The 25 most recent of 68 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 7, 2026No Apparent Adverse Event
IT WAS REPORTED THAT THE DELTA XTEND CENTRAL STOP DRILL IS BLUNT. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25111848 ↗MalfunctionMay 19, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE INSTRUMENT WAS NO LONGER SHARP.
Patient problems: Insufficient Information
MAUDE report 16962485 ↗MalfunctionApr 10, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE CANNULATED STOP DRILL WAS BLUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16706679 ↗MalfunctionFeb 8, 2023Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILL IS DULL AND WILL NOT CUT. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16321794 ↗MalfunctionFeb 1, 2023Device-Device Incompatibility; Device-Device Incompatibility
THIS PC IS RELATED TO (B)(4), WHICH REPORTS ABOUT THE POWER TOOL (CHUCK) USED IN THE SURGERY. THIS PC REPORTS ABOUT THE JOINT/JRN PRODUCT (DRILL) USED IN THE SURGERY. IT WAS REPORTED THAT THIS WAS AN RSA TREATING SHOULDER PERFORMED ON (B)(6) 2023. THE GLENOID CANNULATED STOP DRILL GOT UNABLE TO BE DETACHED FROM THE CHUCK BECAUSE THE GLENOID CANNULATED STOP DRILL WAS FORCIBLY ATTACHED TO THE CHUCK THAT DOES NOT MATCH TO THE GLENOID CANNULATED STOP DRILL. THE PROCEDURE WAS DONE BY USING THE GLENOID CANNULATED STOP DRILL WITH NO PROBLEMS. THERE WAS NO SURGICAL DELAY AND NO HARM TO THE PATIENT. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16277867 ↗MalfunctionDec 9, 2022Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE DAMAGED PEG DRILL COIL NOT FIT OVER METAGLENE GUIDE PIN. THERE WAS A FIVE MINUTE SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15948958 ↗MalfunctionDec 7, 2022Device-Device Incompatibility; Device-Device Incompatibility
INTRAOPERATIVELY, THE CENTRAL DRILL WAS INTRODUCED WITH THE PEG DRILL (7.5MM) OVER THE ALREADY LYING K-WIRE AND THE CENTRAL DRILL CHANNEL WAS PREPARED. WHEN THE DRILL WAS REMOVED, THE CENTRAL K-WIRE JAMMED IN THE DRILL AND COULD NO LONGER BE REMOVED. THE DRILL AND K-WIRE WERE REMOVED FROM THE PATIENT WITHOUT LEAVING ANY REMNANTS. THE REST OF THE SURGICAL PROCEDURE PROCEEDED AS PLANNED. NO PROLONGATION OF THE SURGERY TIME, NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15933613 ↗MalfunctionNov 21, 2022Failure to Cut; Material Integrity Problem; Naturally Worn; Failure to Cut; Material Integrity Problem; Naturally Worn
IT WAS REPORTED THAT THE DRILL IS NOT SHARP, IS DAMAGED. SO THE DEVICE IS NOT PROPERLY IN GOOD CONDITIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15833835 ↗MalfunctionSep 29, 2022Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE PEG DRILL IS GETTING STUCK IN DRILL ATTACHMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15508147 ↗MalfunctionJul 5, 2022Break; Naturally Worn; Break; Naturally Worn
IT WAS REPORTED THAT THE INSTRUMENT WAS REPORTED TO BE BROKEN/WORN OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14914641 ↗MalfunctionJun 14, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT REAMER IS DULL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14686262 ↗MalfunctionMay 10, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE INSTRUMENT WAS FOUND TO BE USEABLE BUT SLIGHTLY BLUNT NO COMPLICATIONS. NO DELAY TO PROCESS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14346795 ↗MalfunctionApr 20, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILLS WERE DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14160199 ↗MalfunctionApr 20, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILLS WERE DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14160196 ↗MalfunctionApr 20, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILLS WERE DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14160193 ↗MalfunctionApr 20, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DRILLS WERE DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14160190 ↗MalfunctionApr 19, 2022Failure to Cut; Failure to Cut
GLENOID CANNULATED STOP DRILL AS IT WAS BLUNT. HUMERAL IMPLANT DRIVER. THE CONNECTION BETWEEN THE DRIVER AND THE TRIAL STEM/PROTHESIS WAS LOOSE DUE TO WEAR AND TEAR. WHEN THE SURGEON REATTACHED THE IMPLANT DRIVER TO THE TRIAL STEM (IN SITU IN THE PATIENTS HUMERUS) IT KEPT PULLING OFF THE TRIAL. SURGICAL DELAY OF 2 MINUTES OCCURRED. NO ADVERSE AFFECTS ON THE PATIENT.
Patient problems: Insufficient Information
MAUDE report 14140934 ↗MalfunctionMar 23, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE GLENOID STEP DRILL AND GLENOID REAMER BLUNT OUT OF CONSIGNMENT SET- NOTED IN CASE TODAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13869293 ↗MalfunctionMar 15, 2022Failure to Cut; Failure to Cut
ADDITIONAL INFORMATION RECEIVED INDICATED THAT THERE WAS A 5-MINUTE SURGICAL DELAY. THE SURGEON USED THE 10MM DRILL BUT DID NOT GO TO THE DEPTH STOP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13771408 ↗MalfunctionFeb 25, 2022Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE DELTA GLENOID CANNULATED STOP DRILL 2307-89-000 WAS DULL EVEN THOUGH IT¿S ONLY BEEN IN THE SET SINCE 2010. A REPLACEMENT IS NEEDED. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13600900 ↗MalfunctionDec 22, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THIS WAS AN UNKNOWN PROCEDURE PERFORMED ON (B)(6) 2021. THE PATIENT HAD THE INFERIOR BONE QUALITY. THE DRILL WAS TOO DULL TO CUT THE LESION. THE PROCEDURE WAS COMPLETED WITH A REPLACING +10MM DRILL WITHOUT A FURTHER ISSUE. THERE WAS NO SURGICAL DELAY AND NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13061286 ↗MalfunctionDec 14, 2021Failure to Cut; Device-Device Incompatibility; Failure to Cut; Device-Device Incompatibility
THE METAGLENE GUIDE PIN GOT STUCK IN THE METAGLENE POSITIONING PLATE. IT SNAPPED OFF IN THE PLATE. THE STAFF WERE UNABLE TO REMOVE THE BROKEN SHARPE END FROM THE PLATE. ITS GONE OFF TO THEIR SSD DEPT AND IF THEY CANT REMOVE IT BE CAREFUL AS IT WILL COME BACK LIKE THAT TO US. THE 2ND METAGLENE GUIDE PIN GOT STUCK IN THE STOP DRILL AND ITS STILL IN THERE AS WELL SO BE CAREFUL WHEN IT COMES BACK. THE STOP DRILL WAS ALSO REPORTED AS BEING BLUNT. THE SURGEON WAS ABLE TO CONTINUE WITH THE CASE AND THANKFULLY WAS HAPPY WITH THE END RESULT OF THE SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13005545 ↗MalfunctionDec 3, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT DURING A DELTA REVERSE TSA, THE SURGEON COMPLAINED THAT THE CENTRAL DRILL WAS DULL. A SECOND SET WAS OPENED AND HE FELT IT WAS ALSO DULL. DURING THE SAME CASE IT WAS NOTED THAT THE DRIVER SHAFT WAS BENT AND WOBBLED. SURGICAL DELAY OF 5 MINUTES.
Patient problems: Insufficient Information
MAUDE report 12923744 ↗MalfunctionDec 3, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT DURING A DELTA REVERSE TSA, THE SURGEON COMPLAINED THAT THE CENTRAL DRILL WAS DULL. A SECOND SET WAS OPENED AND HE FELT IT WAS ALSO DULL. DURING THE SAME CASE IT WAS NOTED THAT THE DRIVER SHAFT WAS BENT AND WOBBLED. SURGICAL DELAY OF 5 MINUTES.
Patient problems: Insufficient Information
MAUDE report 12923705 ↗MalfunctionDec 2, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE CENTRAL METAGLENE DRILL BIT WAS LOOKING BLUNT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12915567 ↗
Other BIT, DRILL devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 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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