R2 QUICK-COMBO 3112-1731Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00653405058086), received between Jun 20, 2018 and Jun 20, 2018 — classified as 2 deaths.

The most frequently reported specific device problem is “Unable to Obtain Readings” (2 reports).

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

• DeathJun 20, 2018Unable to Obtain Readings; Unable to Obtain Readings

  THE USER FACILITY INITIALLY REPORTED THIS INCIDENT AS A "CONNECTION ERROR MESSAGE" AND NO PATIENT INJURY WAS REPORTED. CONMED RECEIVED A COMPLAINT REPORT FROM THE SUPPLIER, IT WAS FOUND THAT THE REPORTED 3112-1731 PAD WOULD NOT WORK DURING A CODE AND WOULD NOT GIVE A READING. THE PATIENT EXPIRED. UPON GATHERING ADDITIONAL INFORMATION, THE INITIAL PRESENTATION OF THE PATIENT WAS PULSELESS AND APNEIC. THE REPORTED PADS WERE CONNECTED TO A LIFEPACK WHICH DISPLAYED CONNECTION ERROR; RHYTHM WOULD INTERMITTENTLY DISPLAY ASYSTOLE. DEFIBRILLATION WAS NOT PROMPTED WHEN A RHYTHM WAS DISPLAYED, AND DEFIBRILLATION WAS NOT ATTEMPTED WITH THE REPORTED PADS. THE FIRST RESPONDERS PROCEEDED WITH CPR AND PRONOUNCED THE PATIENT ON THE FIELD. THIS REPORT IS BEING RAISED ON THE BASIS OF A REPORTED DEATH OF A PATIENT.

  Patient problems: Death

  MAUDE report 7622045 ↗
• DeathJun 20, 2018Unable to Obtain Readings; Unable to Obtain Readings

  THE USER FACILITY INITIALLY REPORTED THIS INCIDENT AS A "CONNECTION ERROR MESSAGE" AND NO PATIENT INJURY WAS REPORTED. CONMED RECEIVED A COMPLAINT REPORT FROM THE SUPPLIER, IT WAS FOUND THAT THE REPORTED 3112-1731 PAD WOULD NOT WORK DURING A CODE AND WOULD NOT GIVE A READING. THE PATIENT EXPIRED. UPON GATHERING ADDITIONAL INFORMATION, THE INITIAL PRESENTATION OF THE PATIENT WAS PULSELESS AND APNEIC. THE REPORTED PADS WERE CONNECTED TO A LIFEPACK WHICH DISPLAYED CONNECTION/DISCONNECTED ERROR; RHYTHM WOULD INTERMITTENTLY DISPLAY ASYSTOLE. THE MONITOR WAS SWITCHED, AND THE SAME ISSUE PRESENTED. DEFIBRILLATION WAS NOT PROMPTED WHEN A RHYTHM WAS DISPLAYED, AND DEFIBRILLATION WAS NOT ATTEMPTED WITH THE REPORTED PADS. THE FIRST RESPONDERS PROCEEDED WITH CPR AND PRONOUNCED THE PATIENT ON THE FIELD. THIS REPORT IS BEING RAISED ON THE BASIS OF A REPORTED DEATH OF A PATIENT.

  Patient problems: Death

  MAUDE report 7621961 ↗