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DRIVEMEDICAL BLS16FBD-ELRRecalls & reported problems

Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K1 Product Description: BlueStreak16"D/L FlipBackArms,Elev,1/ea · 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 00822383293950), received between Sep 26, 2019 and Sep 26, 2019 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use 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.

  • InjurySep 26, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    (B)(6) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. THE DEVICE WAS NOT INVOLVED IN THE INCIDENT. THE PACKAGING WAS INVOLVED IN THE INCIDENT. THE ENDUSER CUT HER HAND ON THE PACKAGING OF THE DEVICE. SHE WAS HOSPITALIZED AND REQUIRED STITCHES.

    Patient problems: Laceration(s)

    MAUDE report 9126464 ↗

Other Wheelchair, mechanical devices

All Wheelchair, mechanical devices →

Sources and updates

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