Kendall SCD 295255Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521129597), received between May 3, 2021 and Jun 27, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fire” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 27, 2024Fire; Fire

  THE CUSTOMER REPORTED THAT WHILE CLEANING THE THEATER, THE ELECTRICAL CORD SHORTED, CAUGHT FIRE, SPARKED, AND SMOKED. THE WALL PANEL ALARMED, INDICATING A HAZARDOUS ELECTRICAL FAULT. THEY CALLED SPOTLESS TO VERIFY. AFTER ONE MINUTE, THE DEVICE THREW A FLAME, SMOKED, AND HAD A LOUD BANG. THERE WAS NO PATIENT IN THE THEATER AT THE TIME OF THE INCIDENT. THE MACHINE WAS PLUGGED IN, BUT IT WAS NOT TURNED ON.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19627287 ↗
• MalfunctionMay 3, 2021Sparking; Sparking

  THE CUSTOMER REPORTED THAT A PATIENT WAS HOOKED UP TO THE SCD COMPRESSION SYSTEM WHEN THE POWER CABLE NEXT TO THE DEVICE SIDE SPARKED AND EXPLODED. THE PATIENT WAS NOT HURT BUT POWER WAS LOST TO THE DEVICE, RCD WAS NOT TRIPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11762235 ↗