PowerPro PRO6042Recalls & reported problems
Conmed Corporation · POWERPRO 5:1 HIGH TORQUE CHUCK ATTACHMENT, 1/4 IN. · Class 1
- 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 10845854018507), received between Jun 25, 2025 and Jun 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 25, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE DISTRIBUTOR REPORTED ON BEHALF OF THE CUSTOMER THAT THE DEVICE, PRO6042 POWERPRO 5:1 HIGH TORQUE CHUCK ATTACHMENT, 1/4 IN. WAS BEING USED ON (B)(6) 2024 AND "THE DEVICE DISASSEMBLED DURING SURGERY.¿ PER FURTHER ASSESSMENT IT WAS FOUND THAT "WHAT WE MEANT BY 'DISASSEMBLED' IS THAT THE COMPONENTS CAME APART FROM THEIR ORIGINAL POSITION, LEAVING THE COUPLING IN TWO SEPARATE PIECES, NO FRAGMENT OR PART REMAINED IN THE SURGICAL SITE." THERE WAS NO IMPACT OR INJURY TO THE PATIENT OR USER. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22327011 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.