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Drive 13220LRecalls & reported problems

Drive Devilbiss Healthcare · Patient RoomSlings Product Description: U-Sling 4pt padded Lg.1/bx · Class 1

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 00822383303543), received between Oct 15, 2019 and Oct 15, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Material Fragmentation1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryOct 15, 2019Material Fragmentation; Material Fragmentation

    DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A SLING USED IN CONJUNCTION WITH A PATIENT LIFT. THIS REPORT IS IN RESPONSE TO A MEDWATCH FORM FORWARDED BY THE NURSING CENTER THAT WAS FORWARDED TO DRIVE, WE HAVE NOT EVALUATED THE SLING TO DATE. WHILE TRANSFERRING A PATIENT USING A MECHANICAL LIFT, THE STRAP ON THE LIFT SLING BROKE RESULTING IN THE RESIDENT FALLING TO THE FLOOR. PATIENT REPORTEDLY SUFFERED FRACTURES.

    Patient problems: Bone Fracture(s)

    MAUDE report 9192395 ↗

Other LIFT, PATIENT, NON-AC-POWERED devices

All LIFT, PATIENT, NON-AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.