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PINNACLE® 601192Recalls & reported problems

B. Braun Medical Inc. · CONTROL MODULE, PINNACLE · Class 2

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 04046964957444), received between Dec 8, 2020 and Dec 8, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Thermal Decomposition of Device” (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

Device problems

  • Thermal Decomposition of Device1

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.

  • MalfunctionDec 8, 2020Thermal Decomposition of Device; Thermal Decomposition of Device

    AS PER REPORTED BY THE USER FACILITY: THE CONTROL PANEL POWER SUPPLY/BRICK CAUGHT FIRE AND MELTED THE POWER RECEPTACLE. IT IS UNKNOWN IF THERE WERE ANY POWER SURGES OR ELECTRICAL ISSUES WITHIN THE WALL OUTLET. IT WAS REPORTED THE TECHNICIAN SAW SMOKE AND UNPLUGGED THE CONTROL PANEL. WHEN THE POWER SUPPLY WAS REMOVED FROM THE CONTROL PANEL THE TECHNICIAN SAW FLAMES WITHIN THE POWER SUPPLY AND THE CONTROL PANEL. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10965674 ↗

Other SYSTEM/DEVICE, PHARMACY COMPOUNDING devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.