3M™ Littmann® Classic III™ 5622Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00707387771898), received between Jan 23, 2019 and Jan 23, 2019 — classified as 1 injury.

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 18, 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.

• InjuryJan 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A FEMALE ALLEGED TWO EAR INFECTIONS ON SEPARATE OCCASIONS AND A RASH ON THE NECK. USE OF A 3M¿ LITTMAN® CLASSIC¿ III MONITORING STETHOSCOPE BEGAN IN (B)(6) 2018. SHE WAS SEEN IN URGENT CARE AND IN THE EMERGENCY ROOM ON SEPARATE OCCASIONS AND WAS TREATED WITH PRESCRIPTION ANTIBIOTICS, AN ORAL STEROID AND EAR DROPS. THE RASH RESOLVED AND THE MOST RECENT EAR INFECTION IS RESOLVING.

  Patient problems: Irritation; Rash; Skin Irritation

  MAUDE report 8272573 ↗