DRIVEMEDICAL SSP18RBDDARecalls & reported problems

Drive Devilbiss Healthcare · Transport/WheelchairReclining Wheelchairs Product Description: SilverSport18"ReclBackDetDesk,1/cs · Class 1

All models of DRIVEMEDICAL (111)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383232072), received between Jan 13, 2020 and Jan 13, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Solder Joint Fracture” (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.

Most reported problems

Device problems

Solder Joint Fracture1

Patient problems

Fall1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

InjuryJan 13, 2020Solder Joint Fracture; Solder Joint Fracture
DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. END-USER WAS RECLINING IN THE CHIR ON HIS PATIO. THE BACK BAR BROKE. HE FELL AND HIT HIS HEAD. HE SOUGHT MEDICAL ATTENTION. HE HAD A BUMP ON THE BACK OF HIS HEAD. NO CAT SCAN OR X-RAYS TAKEN.
Patient problems: Fall
MAUDE report 9583739 ↗

Device details

UDI-DI	`00822383232072`
Brand	DRIVEMEDICAL
Model	SSP18RBDDA
Company	Drive Devilbiss Healthcare
Product code	IOR · Wheelchair, mechanical
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	Not in Commercial Distribution
Record updated	Aug 12, 2024

Device type (GMDN): Attendant-only-propelled wheelchair, non-bariatric

A non-powered wheeled mobility device with a seat designed to enable a healthcare provider/carer to transport a non-bariatric person without the full capacity to walk, typically over short distances and over smooth ground. Often referred to as a transport wheelchair, it is typically designed with four small wheels and includes rear-fitted handles for attendant control of the chair; it does not provide the occupant a mechanism for self-propulsion (it is not a push-rim wheelchair). It provides no function outside of wheeled mobilization.

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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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