PowerPro PRO6047Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854036143), received between Feb 11, 2025 and Feb 11, 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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 11, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  THE DISTRIBUTOR REPORTED ON BEHALF OF THE CUSTOMER THAT THE DEVICE PRO6047 POWERPRO 5:1 ZIMMER/HUDSON REAMER ATTACHMENT, WAS BEING USED ON (B)(6) 2025 AND "THE SHAFT BROKE DURING USE AND BROKE INTO TWO PIECES.¿ PER FURTHER ASSESSMENT, IT WAS FOUND THAT THE DEVICE FRAGMENTS DID FALL INTO THE SURGICAL SITE AND WERE RETRIEVED. THERE WAS NO IMPACT OR INJURY FOR THE PATIENT OR USER. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATE ¿BACKUP INSTRUMENTS¿. 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 21354141 ↗