DRIVEMEDICAL K318DDA-ELRRecalls & reported problems
Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K3 Product Description: Cruiser III,18Lt.Wt,FlipBk,ElvLgRst,1/cs · Class 1
All models of DRIVEMEDICAL (111)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383123363), received between Dec 31, 2020 and Sep 25, 2026 — classified as 1 injury, 1 malfunction.
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
- Detachment of Device or Device Component1
- Naturally Worn1
Patient problems
- Bruise/Contusion1
- Fall1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Detachment of Device or Device Component; Naturally Worn
It was reported that "Wheel chair wheels are worn out and unable to use. Makes its harder to use."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898603 ↗InjuryDec 31, 2020Break; Break
(B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. WE ARE FILING THIS REPORT IN AN OVER-ABUNDANCE OF CAUTION DUE TO AN MDR REGRESSION ANALYSIS. THE BACK OF THE CHAIR BROKE WHILE IN USE CAUSING THE USER TO FALL. HE HIT HIS HEAD AND ARM. NO FURTHER DETAILS TO THE EVENT ARE AVAILABLE.
Patient problems: Bruise/Contusion; Fall
MAUDE report 11100379 ↗
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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