DELTA XTEND 2307-74-014Recalls & reported problems
Depuy (Ireland) · DELTA Xtend PROXIMAL REAMING GUIDE DIA 14 MM · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295116172), received between Aug 10, 2018 and May 11, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
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.
Most reported problems
Device problems
- Break1
- Device-Device Incompatibility1
- Difficult to Remove1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Not Applicable1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 11, 2023Break; Device-Device Incompatibility; Break; Device-Device Incompatibility
IT WAS REPORTED THAT THE INSTRUMENTS BROKE DURING SURGERY AND STUCK TOGETHER. CAN NOT TAKE APART. NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16910811 ↗MalfunctionAug 10, 2018Difficult to Remove; Difficult to Remove
IT WAS REPORTED THAT AFTER PROPERLY ASSEMBLING THE REAMING GUIDE TO THE GUIDE HANDLE, SURGEON INSERTED GUIDE INTO HUMERUS AND WHEN HE TRIED TO UNSCREW THE REAMING GUIDE ROD, THE KNOB ON THE GUIDE ROD BROKE OFF LEAVING ROD STUCK IN GUIDE HANDLE. IT IS UNABLE TO RELEASE THE REAMING GUIDE FROM IT. SURGEON ATTEMPTED TO BEND TIP OF GUIDE ROD TO FREE THE REAMING GUIDE BUT WAS UNSUCCESSFUL. SURGICAL DELAYED 5 MINUTES. ALL PIECES RETRIEVED.
Patient problems: Not Applicable
MAUDE report 7772391 ↗
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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