DRIVEMEDICAL SSP220DDA-SFRecalls & reported problems

Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K2 Product Description: SlvrSprt2 18 SlvrVeinFxdArm.SwgFt,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: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383140506), received between Oct 27, 2022 and Oct 27, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Integrity Problem” (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

Material Integrity Problem1

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.

MalfunctionOct 27, 2022Material Integrity Problem; Material Integrity Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY THE END USERS' MOTHER, WHO STATED "HER DAUGHTER WAS AT SCHOOL THIS PAST WEDNESDAY AND THE CHAIR COLLAPSED ON HER WHILE SITTING IN IT," CAUSING HER TO CUT HER FINGER. THE END USER DID RECEIVE MEDICAL ATTENTION, THE DETAILS OF WHICH ARE CURRENTLY UNKNOWN. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Laceration(s)
MAUDE report 15683344 ↗

Device details

UDI-DI	`00822383140506`
Brand	DRIVEMEDICAL
Model	SSP220DDA-SF
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	Oct 3, 2024

Device type (GMDN): Push-rim manual wheelchair, non-bariatric

A non-powered wheeled personal mobility device with a seat designed to enable a non-bariatric person with a disability, or without the full capacity to walk, to self-mobilize by pushing specially designed rims on the wheels while seated. It is designed with a pair of larger wheels with push-rims attached whereby the occupant propels the device by rotating both wheels; it typically includes rear-fitted handles designed for optional pushing by an attendant. 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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