MEDLINE MDS808200KNMRecalls & reported problems
Medline Industries, Inc. · TRANSPORT CHAIR,BASIC · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00193489038258), received between Jul 3, 2026 and Sep 26, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
- Loose or Intermittent Connection1
- Mechanical Problem1
- Noise, Audible1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2026Noise, Audible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50906433 ↗MalfunctionJul 6, 2026Mechanical Problem
T WAS REPORTED THAT ONE LEGREST WILL NOT LOCK AND THAT THE LEVER IS NOT CORRECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25715817 ↗MalfunctionJul 6, 2026Loose or Intermittent Connection
IT WAS REPORTED THAT "THE CHAIR HAS A STRIPPED HAND SCREW FOR LEFT FRONT WHEEL".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25715563 ↗MalfunctionJul 3, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "THE LEFT FRONT WHEEL WELD UNEXPECTEDLY SNAPPED, CAUSING ME TO FALL FROM THE CHAIR".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25706774 ↗
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
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE MDS808200ABEMedline 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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