DRIVEMEDICAL BLS18FBD-SFRecalls & reported problems
Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K1 Product Description: BlueStreak18"D/L FlipBackArms,SwgFt,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
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383241159), received between Dec 10, 2019 and May 8, 2023 — classified as 2 injuries.
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.
Most reported problems
Device problems
- Break1
- Detachment of Device or Device Component1
Patient problems
- Fall2
- Head Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 8, 2023Break; Break
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT INVOLVING A WHEELCHAIR BY A PROVIDER, WHO REPORTED THAT END USER WAS SITTING ON THE UNIT WHEN IT BROKE AND "HE FELL THROUGH THE CHAIR." THE END USER IS CONTINUING A PHYSICAL THERAPY PROGRAM THAT BEGAN BEFORE THE INCIDENT. THERE WERE NO ADDITIONAL DETAILS ON THE SEVERITY OF THE INJURY PROVIDED WITH THE INITIAL COMPLAINT. DRIVE MADE MULTIPLE ATTEMPTS TO CONTACT THE REPORTER TO INVESTIGATE THE INCIDENT, BUT DID NOT RECEIVE A RESPONSE. DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.
Patient problems: Fall
MAUDE report 16886747 ↗InjuryDec 10, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. THE DEVICE WAS REPAIRED. THE BROKEN UPHOLSTERY WAS DISCARDED. NO EVALUATION CAN BE MAKE ON THE PART. THE END-USER IS A DOUBLE AMPUTEE. THE BACKREST OF THE WHEELCHAIR RIPPED ON BOTH SIDES AND HE ENDED UP FALLING OUT OF THE CHAIR. HE MAY HAVE HIT HIS HEAD. HE WAS BROUGHT TO THE HOSPITAL AND THE DOCTORS SAID HE HAD A STROKE. IT IS UNCLEAR WHETHER HE HAD A STROKE AND FELL OR IF THE EVENT CAUSED THE STROKE. THE PATIENT WAS IN THE HOSPITAL FOR ABOUT 3 WEEKS AND NOW IS IN A REHAB FACILITY. A REPLACEMENT BACK WAS SUPPLIED BY OUR CUSTOMER SERVICE DEPARTMENT AND IT WAS UTILIZED ON THE DEVICE. THE RIPPED BACK UPHOLSTERY WAS DISCARDED. AT THIS TIME NO PICTURES ARE AVAILABLE.
Patient problems: Fall; Head Injury
MAUDE report 9443621 ↗
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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