MDF® MDF747XPBORecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06940211618769), received between Oct 15, 2025 and Oct 15, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

• MalfunctionOct 15, 2025Break; Break

  IT WAS REPORTED FROM THE CUSTOMER: "THAT THE STETHOSCOPE TUBING BROKE ON THE NECK AND SHE STARTED TO FEEL LIKE A BURNING SENSATION. THE CUSTOMER SAID, "THAT THERE IS RASH ON THE NECK TO THE CHEST AND THAT SHE IS TAKING MEDICATION CREAM FOR THE WASHING ON THE NECK." THE CUSTOMER ALSO MENTION THAT "THIS WILL BE THE SECOND TIME THAT THE DOCTOR HAD PRESCRIBE MEDICATION FOR THE RASH AND THE DOCTOR SUGGESTED FOR THE CUSTOMER TO GET IN CONTACT WITH THE STETHOSCOPE COMPANY. THE CUSTOMER MENTION THAT SHE HAD ORDER TWO SLEEVES FOR THE STETHOSCOPES."

  Patient problems: Eczema; Skin Burning Sensation

  MAUDE report 23282947 ↗