3M™ Littmann® Classic II™ 2201Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00707387766160), 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, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  A MALE REPORTED AN ALLEGED INJURY OF THE RIGHT TYMPANIC MEMBRANE AFTER AN EAR TIP FELL OFF A 3M¿ LITTMAN® CLASSIC¿ II S.E. STETHOSCOPE. THE STETHOSCOPE WAS USED FOR APPROXIMATELY ONE WEEK. OUTPATIENT CARE WAS RECEIVED AND THE EARDRUM PUNCTURE RECOVERED; HOWEVER, THERE IS A LITTLE DIFFERENCE IN HEARING PERFORMANCE NOTICED BETWEEN THE LEFT AND RIGHT EAR.

  Patient problems: Hearing Impairment

  MAUDE report 8272669 ↗