DELTA XTEND 2407-89-015Recalls & reported problems
Depuy (Ireland) · DELTA Xtend GLENOID CANNULATED STOP DRILL DIA 7.5MM+15MM · Class 1
All models of DELTA XTEND (194)
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 10603295285977), received between Sep 29, 2017 and Feb 23, 2021 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (3 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.
Most reported problems
Device problems
- Failure to Cut3
- Appropriate Device Problem Term/Code Not Available1
- Dull, Blunt1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 23, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE GLENOID DRILLS WERE TOO DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11367234 ↗MalfunctionFeb 18, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE GLENOID DRILLS WERE TOO DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11345253 ↗MalfunctionFeb 18, 2021Failure to Cut; Failure to Cut
IT WAS REPORTED THAT THE SURGEON COMPLAINED THAT THE GLENOID DRILLS WERE TOO DULL. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11345084 ↗MalfunctionJul 29, 2020Dull, Blunt; Dull, Blunt
ADDITIONAL INFORMATION RECEIVED STATED THAT THE EVENT HAPPENED DURING STERILIZATION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10340886 ↗MalfunctionSep 29, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT THE (B)(6) TECHNICIAN REPORTED A DEFECT WITH THE GUIDE PINS. THE PRODUCTS DO NOT SLIDE THROUGH PRODUCT CODE 230789015 DURING FUNCTIONALITY TESTING. THE PARTS ARE BLOCKED HALF WAY THROUGH. THIS ISSUE INVOLVES PRODUCTS THAT HAVE NEVER BEEN USED.
Patient problems: No Information
MAUDE report 6903779 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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