DELTA XTEND 2307-86-002Recalls & reported problems
Depuy (Ireland) · DELTA Xtend V SHAPE GLENOID RETRACTOR · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295116417), received between Jun 4, 2018 and Mar 12, 2025 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Break” (7 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
- Break7
- Material Deformation4
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Insufficient Information1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 12, 2025Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED THAT THE SHOULDER INSTRUMENTS ARE BROKEN, BENT, AND STRIPPED. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21586367 ↗MalfunctionMar 12, 2025Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED THAT THE SHOULDER INSTRUMENTS ARE BROKEN, BENT, AND STRIPPED. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21586366 ↗MalfunctionMar 12, 2025Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED THAT THE SHOULDER INSTRUMENTS ARE BROKEN, BENT, AND STRIPPED. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21586363 ↗MalfunctionMar 12, 2025Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED THAT THE SHOULDER INSTRUMENTS ARE BROKEN, BENT, AND STRIPPED. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21586332 ↗MalfunctionDec 29, 2023Break; Break
IT WAS REPORTED THAT ALL OF THE PRODUCTS BROKE DURING THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18416908 ↗MalfunctionAug 30, 2023Break; Break
IT WAS REPORTED THAT THE GLENOID RETRACTOR BROKE. IT WAS UNKNOWN ABOUT SURGICAL DELAY.
Patient problems: Insufficient Information
MAUDE report 17656258 ↗MalfunctionJun 4, 2018Break; Break
IT WAS REPORTED THAT THE INSTRUMENTS BROKE DURING SURGERY. NO SURGICAL DELAY. ALL PIECES WERE RETRIEVED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7565649 ↗
Other RETRACTOR devices
- Endo Paddle Retract 173046Covidien LP · RETRACTOR56 reports
- Omni-Tract® 4040Integra Lifesciences Corporation · RETRACTOR1 recall3 reports
- Omni-Tract® 11275Integra Lifesciences Corporation · RETRACTOR1 recall2 reports
- RadiaLux™ 50-101-1Medtronic Navigation, Inc. · RETRACTOR1 recall2 reports
- CHARNLEY 9620-04-000Depuy International Ltd · RETRACTOR1 recall2 reports
- NA 2176-10-000Depuy (Ireland) · RETRACTOR51 reports
- Fathom MR2-102050Seaspine Orthopedics Corporation · RETRACTOR1 recall1 report
- Omni-Tract® 11303RIntegra Lifesciences Corporation · RETRACTOR1 recall0 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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