MEDLINE INDUSTRIES, INC. MDS808200F3SRecalls & reported problems
Medline Industries, Inc. · WHEELCHAIR,TRANSPORT,ULTRALGHT 3,SILVER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00884389102483), received between Jun 16, 2026 and Sep 30, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (2 reports).
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
- Material Twisted/Bent2
- Activation Failure1
- Activation Problem1
- Detachment of Device or Device Component1
- Mechanics Altered1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Twisted/Bent
It was reported that "the screw on the left side of the transport chair handle is bent. Stated that it is on the back of the chair, and it is the screw that attaches the flap piece."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946501 ↗MalfunctionSep 29, 2026Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938011 ↗MalfunctionSep 28, 2026Activation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916081 ↗MalfunctionSep 24, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50889605 ↗MalfunctionJun 19, 2026Mechanics Altered
IT WAS REPORTED THAT THE TRANSPORT CHAIR RECEIVED WITH LEFT OR RIGHT SIDE BRAKE NOT LOCKING. BRAKE SHOE IS NOT ENGAGING IN WHEEL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25568188 ↗MalfunctionJun 16, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT "THE WHEEL OF THE CHAIR CAME OFF."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25524683 ↗
Other Wheelchair, mechanical devices
- MEDLINE K1186N22SMedline Industries, Inc. · Wheelchair, mechanical48 reports
- Guardian K4186N24EMedline Industries, Inc. · Wheelchair, mechanical22 reports
- MEDLINE INDUSTRIES, INC. MDS808650Medline Industries, Inc. · Wheelchair, mechanical18 reports
- Medline MDS806850Medline Industries, Inc. · Wheelchair, mechanical17 reports
- Quickie 7 SeriesSunrise Medical (US) LLC · Wheelchair, Mechanical1 death10 reports
- Guardian K3186N24EMedline Industries, Inc. · Wheelchair, mechanical10 reports
- Guardian K3206N24SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- MEDLINE K3186N34SMedline Industries, Inc. · Wheelchair, mechanical9 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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