Medline MDS926301Recalls & reported problems
Medline Industries, Inc. · STETHOSCOPE,SPRAGUE RAPPAPORT,BLACK · 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 00080196717067), received between Sep 26, 2026 and Sep 26, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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
- Incorrect, Inadequate or Imprecise Result or Readings1
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 26, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50906374 ↗
Other STETHOSCOPE, MANUAL devices
- 3M™ Littmann® Classic III™ 56223m Company · STETHOSCOPE, MANUAL1 report
- Medline MDS92250Medline Industries, Inc. · 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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