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RELIANCE 48360210Recalls & reported problems

Stryker Corporation · OSTEOTOME CURVED · Class 1

All models of RELIANCE (9)

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 07613327268379), received between Sep 15, 2017 and Sep 15, 2017 — 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

Patient problems

  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence 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 15, 2017Material Deformation

    IT WAS REPORTED THAT; SURGEON USED CHISEL TO CUT THE FACET JOINT! THE CUTTING EDGE CAME OUT DEFORMED. THE FACET JOINT WAS CUT AND TAKEN OUT WITH ANOTHER CHISEL THAT THE HOSPITAL OWNED. NO DEFORMITY OF THE SECOND CHISEL.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 6870020 ↗

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Sources and updates

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