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DELTA XTEND 2307-81-003Recalls & reported problems

Depuy (Ireland) · DELTA Xtend PROXIMAL REAMER FOR MONOBLOC IMPLANT SZ 1 · 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 10603295116325), received between Jan 28, 2019 and Jan 29, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (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.

Most reported problems

Device problems

  • Dull, Blunt2

Patient problems

  • No Consequences Or Impact To Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 29, 2019Dull, Blunt; Dull, Blunt

    THE REAMER IS DULL AND THE SURGEONS HAVE HAD TO MAKE SO MUCH FORCE FRACTURED THE BONE, ALSO THE REAMER OF THE STEM IS DULL. AND THE SCREWED SCREW DRIVER DOES NOT TAKE THE SCREW.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8284779 ↗
  • MalfunctionJan 28, 2019Dull, Blunt; Dull, Blunt

    DEVICE IS DULL.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8282846 ↗

Other REAMER devices

All REAMER devices →

Sources and updates

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