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CORE, Maestro 5400207000Recalls & reported problems

Stryker Corporation · Non-exhausting Footpedal · Class 2

All models of CORE, Maestro (4)

Data updated Oct 16, 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 07613154284467), received between Jul 24, 2018 and Jan 22, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (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

  • Leak/Splash1
  • Physical Resistance/Sticking1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionJan 22, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT IN WHICH THE DEVICE HAD A STICKY SAFETY DEVICE THAT COULD LEAD TO UNINTENDED POWER-UP. - 1 EVENT HAD NO PATIENT INVOLVEMENT; NO PATIENT IMPACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11215223 ↗
  • MalfunctionJul 24, 2018Leak/Splash; Leak/Splash

    THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS IN WHICH THE DEVICE WAS REPORTEDLY LEAKING. TWO EVENTS HAD NO PATIENT INVOLVEMENT; NO PATIENT IMPACT.

    Patient problems: No Patient Involvement

    MAUDE report 7714829 ↗

Other MOTOR, DRILL, PNEUMATIC devices

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Sources and updates

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