McKesson 146-SSP18RBDDARecalls & reported problems
Mckesson Medical-Surgical Inc. · Full Reclining Wheelchair, 18 Inches DETACHABLE DESK ARMS | SWING-AWAY ELEVATING LEG RESTS · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 2
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00612479223363), received between Oct 15, 2025 and Nov 10, 2025 — classified as 2 deaths.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information2
Patient problems
- Strangulation2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
DeathNov 10, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A DRIVE WHEELCHAIR AND UNIDENTIFIED LAP BELT BY A LETTER FROM AN ATTORNEY ALLEGING THE END USER PASSED AWAY AFTER SLIDING DOWN IN THE WHEELCHAIR TO THE FLOOR, CAUSING THE LAP BELT TO BECOME TIGHT AROUND HER NECK LEADING TO ASPHYXIATION. INFORMATION PROVIDED BY THE ATTORNEY INDICATES THE LAP BELT WAS MANUFACTURED BY BELT INC AND NOT DISTRIBUTED BY DRIVE DERVILBISS HEALTHCARE. AN UPDATE WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Strangulation
MAUDE report 23507918 ↗DeathOct 15, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A DRIVE WHEELCHAIR AND UNIDENTIFIED LAP BELT BY A LETTER FROM AN ATTORNEY ALLEGING THE END USER PASSED AWAY AFTER SLIDING DOWN IN THE WHEELCHAIR TO THE FLOOR, CAUSING THE LAP BELT TO BECOME TIGHT AROUND HER NECK LEADING TO ASPHYXIATION. INFORMATION PROVIDED BY THE ATTORNEY INDICATES THE LAP BELT WAS MANUFACTURED BY BELT INC AND NOT DISTRIBUTED BY DRIVE DERVILBISS HEALTHCARE. AN UPDATE WILL BE FILED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Strangulation
MAUDE report 23304272 ↗
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
- MEDLINE K3186N34SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- Guardian K3206N24SMedline 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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