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Precision Falcon 6725137105Recalls & reported problems

Stryker Corporation · Oscillating Tip Saw Cartridge · Class 1

All models of Precision Falcon (6)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327143775), received between Dec 18, 2018 and May 10, 2021 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Device problems

  • Break2
  • Fracture1

Patient problems

  • No Consequences Or Impact To Patient2
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 10, 2021Fracture; Fracture

    IT WAS REPORTED THAT DURING A SURGICAL PROCEDURE, THE BLADE BROKE. IT WAS FURTHER REPORTED THAT BROKEN PIECE WAS RETRIEVED FROM THE PATIENT. IT WAS ALSO REPORTED THAT THERE WERE NO ADVERSE CONSEQUENCES AND NO DELAYS AS A RESULT OF THIS EVENT. IT WAS FURTHER REPORTED THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11798098 ↗
  • MalfunctionDec 18, 2018Break; Break

    IT WAS REPORTED THAT DURING A TOTAL KNEE ARTHROPLASTY THAT TWO PRECISION BLADES BROKE AT THE CONTACT POINT OF THE PRECISION SAW. IT WAS FURTHER REPORTED THAT THERE WAS A SHORT DELAY TO GET A NEW BLADE. IT WAS ALSO REPORTED THAT THERE WERE NO ADVERSE CONSEQUENCES AND THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THIS REPORT IS FOR THE SECOND BLADE THAT BROKE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8176000 ↗
  • MalfunctionDec 18, 2018Break; Break

    IT WAS REPORTED THAT DURING A TOTAL KNEE ARTHROPLASTY THAT TWO PRECISION BLADES BROKE AT THE CONTACT POINT OF THE PRECISION SAW. IT WAS FURTHER REPORTED THAT THERE WAS A SHORT DELAY TO GET A NEW BLADE. IT WAS ALSO REPORTED THAT THERE WERE NO ADVERSE CONSEQUENCES AND THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THIS REPORT IS FOR THE FIRST BLADE THAT BROKE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8175993 ↗

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Sources and updates

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