Drive SSP218DDA-ELRRecalls & reported problems

Drive Devilbiss Healthcare · SlvrSprt2,18"SlvrVeinDetDskArm,ElvLg1/cs · Class 1

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 00822383140452), received between Dec 2, 2020 and Dec 2, 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

Laceration(s)1

Recent adverse event reports

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

InjuryDec 2, 2020Solder Joint Fracture; Solder Joint Fracture
DRIVE DEVILBISS HEALTHCARE 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 PRODUCT WAS NOT RETURNED FOR EVALUATION BY THE END USER. DEVICE WAS IN USE WHEN THE WELD BROKE. THE USER WAS INJURED ON HER LOWER LEFT EXTREMITY. ADDITIONAL DETAILS ARE NOT AVAILABLE. HISTORICAL DATA FOR THESE COMPLAINTS OF THE SAME NATURE WAS REVIEWED AND FOUND VERY LIMITED REPORTING WHICH SHOWS NO TREND.
Patient problems: Laceration(s)
MAUDE report 10936654 ↗

Device details

UDI-DI	`00822383140452`
Brand	Drive
Model	SSP218DDA-ELR
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	In Commercial Distribution
Record updated	Jun 22, 2026

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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All Wheelchair, mechanical devices →

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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