Medline MDS9750Recalls & reported problems
Medline Industries, Inc. · STETHOSCOPE,TEACHING,TWO-BINAURALS · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00080196720265), received between Sep 15, 2026 and Sep 15, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (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
- Material Integrity Problem1
- Output Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Material Integrity Problem; Output Problem
It was reported that "these stethoscopes do not work. Our instructors and students can¿t hear out of them."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50774986 ↗
Other STETHOSCOPE, MANUAL devices
- Medline MDS926301Medline Industries, Inc. · STETHOSCOPE, MANUAL1 report
- 3M™ Littmann® Classic III™ 56223m Company · STETHOSCOPE, MANUAL1 report
- Medline MDS92250Medline 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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