DELTA XTEND 2307-73-003Recalls & reported problems
Depuy (Ireland) · DELTA Xtend SUPERIOR LATERAL CUTTING GUIDE · 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 10603295116103), received between Jun 5, 2023 and Jul 11, 2025 — classified as 4 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.
Reports received per month
Most reported problems
Device problems
- Break1
- Device-Device Incompatibility1
- Material Deformation1
- Material Integrity Problem1
- Mechanical Jam1
- Mechanical Problem1
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.
MalfunctionJul 11, 2025Mechanical Problem; Device-Device Incompatibility; Mechanical Problem; Device-Device Incompatibility
IT WAS REPORTED THE SCREW IN THE SUPERIOR LATERAL CUTTING JIG WOULD NOT TIGHTEN TO HOLD IN PLACE. THE SURGEON FREE HAND CUT THE HUMERAL HEAD. THERE WAS NO SURGICAL DELAY OR HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22479762 ↗MalfunctionJun 10, 2025Mechanical Jam; Mechanical Jam
THE GUIDE BECAME ¿JAMMED¿ AFTER THE BLUE SCREW, WHICH TIGHTENS AND SECURES THE CUTTING GUIDE PLATE COLD-WELDED. THE SURGEON WAS UNABLE TO REMOVE THE CUTTING GUIDE PLATE TO MAKE HIS HUMERAL HEAD CUT; THE SURGEON HAD TO COMPLETE THIS STAGE ¿FREE-HAND¿. SURGERY TIME WAS INCREASED BY TEN MINUTES. THERE WAS NO HARM TO THE PATIENT AS THE SURGEON WAS ABLE TO CARRY OUT AN ALTERNATIVE SOLUTION TO THE ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22175808 ↗MalfunctionNov 19, 2024Material Deformation; Material Integrity Problem; Material Deformation; Material Integrity Problem
ADDITIONAL INFORMATION WAS RECEIVED AND STATED THAT THE DEVICE WAS A CONSIGNMENT INSTRUMENT. THE SCREW WAS CROSS-THREADED AND DAMAGED. UNABLE TO BE USED AND HAS BEEN RETURNED TO THE DEPOT. THE DEVICE WAS CONFIRMED NOT BROKEN INTO 2 PIECES. NO SURGICAL DELAYS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20725700 ↗MalfunctionJun 5, 2023Break; Break
IT WAS REPORTED THAT ON OPENING THE DELTA XTEND INSTRUMENT TRAY THAT THE BLUE SCREW ON THE SUPERIOR LATERAL CUTTING GUIDE WAS MISSING. IT APPEARED TO HAVE SHEARED OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17062640 ↗
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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