MEDLINE INDUSTRIES, INC. MDS806750Recalls & reported problems
Medline Industries, Inc. · WHEELCHAIR,EXCEL,20" W,RDLA,ELR · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00080196132853), received between Aug 7, 2026 and Sep 24, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Fracture1
- Incomplete or Missing Packaging1
- Loose or Intermittent Connection1
- Mechanics Altered1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Mechanics Altered
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890373 ↗MalfunctionAug 10, 2026Incomplete or Missing Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50193534 ↗MalfunctionAug 10, 2026Loose or Intermittent Connection
It was reported that the wheelchair arrived with an issue of one of the rear wheels not moving correctly and they believe it may be an issue with the bearing.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50191759 ↗MalfunctionAug 10, 2026Fracture
It was reported that there was shipping damage to the box upon arrival and the customer noticed when they first went to test the wheelchair that they were having difficulty with the wheels moving.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50191726 ↗MalfunctionAug 7, 2026Break
It was reported that the wheelchair arrived as damaged. One box had damaged wheelchair inside and it was discovered it was broken; one of the wheel spokes had broke off.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50180304 ↗
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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