Drive 13224XLRecalls & reported problems
Drive Devilbiss Healthcare · Patient RoomSlings Product Description: Sling Full Body XL Solid 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 00822383109404), received between Feb 3, 2025 and Feb 3, 2025 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Integrity Problem1
Patient problems
- Hip Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 3, 2025Material Integrity Problem; Material Integrity Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A PATIENT LIFT SLING VIA A PROVIDER'S VOLUNTARY MEDWATCH REPORT, WHICH STATED THE SLING ON A PATIENT LIFT BROKE DURING TRANSPORT, CAUSING THE PATIENT TO FALL TO THE FLOOR AND SUSTAIN A HIP FRACTURE. THE REPORT DID NOT IDENTIFY HOW THE SLING BROKE, AND EFFORTS TO CONTACT THE PROVIDER TO GATHER ADDITIONAL INFORMATION HAVE BEEN UNSUCCESSFUL. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT IF THE MANUFACTURER CAN BE IDENTIFIED.
Patient problems: Hip Fracture
MAUDE report 21293241 ↗
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- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
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- Viking™ L mobile lift 2040044Liko AB · Lift, patient, non-ac-powered1 recall4 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.