MEDLINE INDUSTRIES, INC. MDS808200Recalls & reported problems
Medline Industries, Inc. · WHEELCHAIR,TRANSPORT,19" · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00080196733401), received between Jun 15, 2026 and Sep 24, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
- Mechanical Jam1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Mechanical Problem
It was reported that "THE FOOT PEDAL ON THE RIGHT SIDE IS NOT WORKING IT DOES NOT HOOK ON CHAIR."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50888504 ↗MalfunctionSep 23, 2026Mechanical Jam
It was reported that "The legrest push button's are jammed and he cannot adjust the height of the legrest."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50867417 ↗MalfunctionJun 15, 2026Insufficient Device Problem Information
IT WAS REPORTED THAT THE FRONT WHEELS ARE NO LONGER TURNING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25503272 ↗
Other CHAIR, WITH CASTERS devices
- MEDLINE MDS808210AREMedline Industries, Inc. · CHAIR, WITH CASTERS115 reports
- MEDLINE MDS808210ABEMedline Industries, Inc. · CHAIR, WITH CASTERS75 reports
- Zippie Voyage Voyage; Voyage VIPSunrise Medical (US) LLC · Chair, With Casters1 recall9 reports
- Ki TykeKi Mobility, LLC · Chair, With Casters1 recall0 reports
- MEDLINE MDS808200KDMedline Industries, Inc. · CHAIR, WITH CASTERS22 reports
- MEDLINE MDS808200ABEMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE TCB228N21SMedline Industries, Inc. · CHAIR, WITH CASTERS6 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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