DELTA XTEND 2307-84-001Recalls & reported problems
Depuy (Ireland) · DELTA Xtend LOCKING WRENCH FOR MODULAR IMPLANT DIA 10-12MM · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295116370), received between Oct 12, 2023 and Oct 12, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
- Improper or Incorrect Procedure or Method1
- Scratched Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 12, 2023Improper or Incorrect Procedure or Method; Scratched Material; Improper or Incorrect Procedure or Method; Scratched Material
WHEN IN PREPARATION TO TIGHTEN THE DELTA EXTEND STEM TO THE EPIPHYSIS WE NOTICED THAT THE SIZE 10-12 SPANNER WAS NOT IN THE SET EXCEPT THERE WERE 2 OF THE SIZE 6-8 SPANNERS. AS A RESULT, WHEN TIGHTENING THE TWO PROSTHESIS, SOME OF THE HA COATING WAS SCRATCHED AS WE USED THE SIZE 8 WHICH WAS JUST TOO SMALL TO DO THE JOB CORRECTLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17924042 ↗
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- RECLAIM 2975-00-300Depuy (Ireland) · WRENCH51 reports
- PINNACLE 2217-50-006Depuy (Ireland) · WRENCH34 reports
- NA 388.261Synthes GmbH · WRENCH32 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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