DELTA XTEND 2307-76-001Recalls & reported problems
Depuy (Ireland) · DELTA Xtend ECCENTRIC PROXIMAL REAMING ADAPTATOR SZ 1 · Class 1
All models of DELTA XTEND (194)
Data updated Oct 16, 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 10603295116202), received between Sep 17, 2018 and Sep 17, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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 16, 2026.
Most reported problems
Device problems
- Material Deformation1
- Material Twisted/Bent1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2018Material Deformation; Material Twisted/Bent; Material Deformation; Material Twisted/Bent
COMPLAINT DESCRIPTION: IT WAS REPORTED THAT THE EPI 1 TOP HAT WOULD NOT FILL OVER THE SLEEVES AND GOT STUCK DURING SURGERY. INVESTIGATION METHOD: (B)(6) 2017: COMPLAINT SAMPLE DEVICES SHIPPED BY (B)(6). AWB# TO BE DETERMINED. (B)(6). INVESTIGATION SUMMARY: IT WAS REPORTED THAT THE EPI 1 TOP HAT WOULD NOT FILL OVER THE SLEEVES AND GOT STUCK DURING SURGERY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7882485 ↗
Other REAMER devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 reports
- QUICKSET 2440-00-553Depuy (Ireland) · REAMER1,105 reports
- QUICKSET 2440-00-547Depuy (Ireland) · REAMER1,073 reports
- QUICKSET 2440-00-555Depuy (Ireland) · REAMER1,065 reports
- QUICKSET 2440-00-557Depuy (Ireland) · REAMER1,031 reports
- QUICKSET 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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