Kendall 33506 (UDI 10884527021468)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884527021468), received between Jul 22, 2025 and Jul 22, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Overheating 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• MalfunctionJul 22, 2025Overheating of Device; Overheating of Device

  THE CUSTOMER REPORTED THAT ONE (1) EACH OF THE GE ADAPTER SKU 33506'S INTERNAL GREEN AND WHITE PLASTIC MOLDING HAS MELTED AND COME APART FROM THE PINK CASING. ADDITIONAL INFORMATION RECEIVED ON 09JUL2025 STATED THAT ONLY 33506 IS AFFECTED. UNFORTUNATELY, THEY HAD NO LOT # NOR A SAMPLE. THEY SAID IT HAPPENED A WHILE AGO AND ONLY HAD A PICTURE. IT IS NOT KNOWN HOW LONG IT'S BEEN USED. THE REP IS NOT AWARE OF ANY HEATING ISSUES WITH THE PRODUCT OR MONITOR DURING USE OR WHEN THIS ADAPTER IS CONNECTED TO THE MONITOR SOCKET.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22564263 ↗