MICROPOWER 00602102100Recalls & reported problems
Conmed Corporation · Micropower Medium Speed Drill, Permanent Lever · Class 2
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 10845854013182), received between Jun 18, 2019 and Jun 18, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (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
- Mechanical Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 18, 2019Mechanical Problem; Mechanical Problem
THE CONMED REPRESENTATIVE REPORTED ON BEHALF OF THE FACILITY THAT THE 00602102100, MICROPOWER MEDIUM SPEED DRILL, WOULD NOT LOCK AND RELEASED THE BUR (CONCOMITANT DEVICE) AND IT DROPPED INTO THE HUMERAL SHAFT DURING A REVERSE SHOULDER ARTHROPLASTY ON (B)(6) 2019. IT WAS BEING USED TO MAKE THE HUMERAL CUT AND DO SOME BURRING OF THE BONE OFF THE HUMERAL SHAFT. THE BUR FELL OUT OF THE DRILL HAND PIECE A FEW TIMES SO THE SURGICAL TEAM WAS SURE TO LOCK THE DRILL, BUT THE BUR STILL FELL OUT AND HAD TO BE RETRIEVED. IT WAS UNCLEAR IF THE HAND PIECE WAS OPERATED WITH THE BUR GUARD AS INDICATED. THE SURGEON HAD TO USE AN IMAGE INTENSIFIER TO X-RAY AND LOCATE THE BUR. THIS ADDED AN ADDITIONAL 2 HOURS TO THE CASE. THE BUR WAS LOCATED AND REMOVED INTACT USING LONG GRASPERS. THE SURGERY WAS OTHERWISE COMPLETED AS PLANNED AND WITHOUT FURTHER INCIDENT. THERE WAS NO PATIENT INJURY REPORTED. THIS REPORT IS BEING RAISED BASED ON DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8708331 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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