DELTA XTEND 2307-20-101Recalls & reported problems
Depuy (Ireland) · DELTA Xtend MODULAR CENTERED EPIPHYSIS TRIAL SZ 1 · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295115717), received between Dec 29, 2022 and May 21, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (2 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
- Break2
- Device-Device Incompatibility2
- Naturally Worn2
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2024Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
ADDITIONAL INFORMATION RECEIVED: A. WAS THERE ANY PATIENT HARM/CONSEQUENCE RELATED TO THE EVENT? NO B. WAS THERE ANY SURGICAL DELAY RELATED TO THE EVENT? NO C. CAN YOU PLEASE CLARIFY WHAT DO YOU MEAN BY ¿DAMAGED¿? WAS IT WORN, CRACKED, BROKEN INTO PIECES, BENT, STRIPPED, CROSS THREADED OR ANY DEVICE INTERACTION. WORN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19367998 ↗MalfunctionJan 25, 2024Break; Break
IT WAS REPORTED THAT DEVICE WAS DEFECTIVE, NO PATIENT CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18580038 ↗MalfunctionOct 11, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
IT WAS REPORTED THAT THE INSTRUMENT IS NO LONGER FUNCTIONAL DUE TO WEAR AND TEAR. NO EFFECT ON PATIENT OR SURGERY TIME. PLEASE NOTE THAT INSTRUMENT DOES NOT ENGAGE EFFICIENTLY WITH DISTAL TRAIL STEM COMPONENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17914362 ↗MalfunctionDec 29, 2022Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component
DELTA XTEND LOCKING SCREWDRIVER WAS MISSING ONE OF THE 'CASTLES' THAT CONNECTS THE HANDLE TO THE SCREW. WAS PICKED UP AT THE BEGINNING OF THE CASE UPON INSPECTION. EPIPYHSIS TRIAL WAS MISSING THE SCREW THAT LOCKS IT TO THE STEM TRIAL; THIS ALSO WAS PICKED UP AT THE BEGINNING OF THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16069541 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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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