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S-NW CAN-Bus 30264000Recalls & reported problems

W & H Dentalwerk Bürmoos GmbH · Foot Control · Class 1

Data updated Oct 18, 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 J021302640001), received between May 9, 2018 and May 9, 2018 — classified as 1 malfunction.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • 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.

  • MalfunctionMay 9, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    A DENTIST OF THE (B)(6) DR. (B)(6) CLINIC COMPLAINED THAT THE MOTOR OF THE "IMPLANTMED" IS STILL WORKING AFTER HE RELEASES THE FOOT PEDAL. THERE WAS NO INJURY IN THIS CASE, HOWEVER, IT MUST BE PRESUMED THAT RECURRENCE OF THIS MALFUNCTION COULD POSSIBLY CAUSE OR CONTRIBUTE TO A SERIOUS INJURY OR REQUIRE MEDICAL OR SURGICAL INTERVENTION TO PRECLUDE PERMANENT INJURY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7497854 ↗

Other Controller, Foot, Handpiece And Cord devices

All Controller, Foot, Handpiece And Cord devices →

Sources and updates

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