Medline MDS92250Recalls & reported problems
Medline Industries, Inc. · STETHOSCOPE, ADULT, STNLSS STL,GRY · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00080196326313), received between Sep 2, 2025 and Sep 2, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Damaged Thread” (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.
Reports received per month
Most reported problems
Device problems
- Damaged Thread1
- Sharp Edges1
Patient problems
- Laceration(s)1
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 2, 2025Sharp Edges; Damaged Thread; Sharp Edges; Damaged Thread
ACCORDING TO THE CUSTOMER, ON (B)(6) 2025, THE USER PLACED THE STETHOSCOPE TO THEIR EARS WITHOUT KNOWING THE "EAR BUD HAD FALLEN OFF" RESULTING IN A LACERATION OF THE LEFT EAR CANAL AND PERFORATED TYMPANIC MEMBRANE. THE CUSTOMER STATED THAT THE USER WENT TO URGENT CARE AND AN ENT PROVIDER FOR TREATMENT AND COMPLAINED OF SEVERE PAIN, RINGING IN THE EAR, MUFFLED HEARING, AND BLEEDING.
Patient problems: Laceration(s); Perforation
MAUDE report 22936859 ↗
Other STETHOSCOPE, MANUAL devices
- Medline MDS926301Medline Industries, Inc. · STETHOSCOPE, MANUAL1 report
- 3M™ Littmann® Classic III™ 56223m Company · STETHOSCOPE, MANUAL1 report
- Medline MDS9750Medline Industries, Inc. · STETHOSCOPE, MANUAL1 report
- Medline MDS9543CSMedline Industries, Inc. · STETHOSCOPE, MANUAL1 report
- Medline MDS926201CSMedline Industries, Inc. · STETHOSCOPE, MANUAL1 report
- Medline MDS926101CSMedline Industries, Inc. · STETHOSCOPE, MANUAL1 report
- MDF® MDF747XPBOMDF Instruments Medifriend Inc. · Stethoscope, Manual1 report
- 3M™ Littmann® Classic II™ 22013m Company · STETHOSCOPE, MANUAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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