MEDLINE K1186N13SRecalls & reported problems
Medline Industries, Inc. · WC,K1,18",FLPA,SA, 300 LB · Class 1
Data updated Oct 16, 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 10193489001020), received between May 12, 2026 and Sep 24, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Fracture” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
- Material Twisted/Bent2
- Material Integrity Problem1
- No Apparent Adverse Event1
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 24, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50883164 ↗MalfunctionSep 23, 2026Material Twisted/Bent
It was reported that "they received a damaged chair from this order."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869493 ↗MalfunctionAug 11, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50216357 ↗MalfunctionMay 21, 2026Material Integrity Problem
PER REPORT, "THE FACILITY RECEIVED A BROKEN WHEEL; PLEASE ASSIST WITH THE RETURN OF THIS ITEM."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25250509 ↗MalfunctionMay 20, 2026Fracture
IT WAS REPORTED UPON DELIVERY, THE WHEELCHAIR HAD A CRACK ON ONE OF THE REAR WHEEL SPOKES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25229110 ↗MalfunctionMay 12, 2026No Apparent Adverse Event
CUSTOMER STATED, "THE WHEEL IS DAMAGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25153895 ↗
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
- Guardian K3186N24EMedline Industries, Inc. · Wheelchair, mechanical10 reports
- Quickie 7 SeriesSunrise Medical (US) LLC · Wheelchair, Mechanical1 death10 reports
- Guardian K3206N24SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- MEDLINE KX228V21EMedline 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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