Drive 13223MRecalls & reported problems
Drive Devilbiss Healthcare · Patient RoomSlings Product Description: Sling Full Body Med Mesh 1/bx · Class 1
Data updated Oct 16, 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 00822383103679), received between Feb 13, 2025 and Sep 18, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (2 reports).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Split, Cut or Torn2
Patient problems
- Bone Fracture(s)1
- Wound Dehiscence1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 18, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A PATIENT LIFT SLING BY THE PROVIDER WHO STATED THAT THE STRAP SNAPPED, AND THE END USER FELL, REOPENING A WOUND ON THEIR LEG. THE RIGHT ABOVE THE KNEE AMPUTATION SITE, THAT WAS REOPENED, HAD ANTIBIOTICS APPLIED TO THE SITE WITH BANDAGES. PRODUCT LABELING STATES, "INSPECT PATIENT SLINGS FOR WEAR PRIOR TO EACH USE. IF SIGNS OF TEARING, FRAYING OR WEAR ARE FOUND DISCARD THE SLING IMMEDIATELY; WORN OUT SLINGS ARE NOT SAFE FOR USE AND MAY RESULT IN INJURY OR DEATH." AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Wound Dehiscence
MAUDE report 23084764 ↗InjuryFeb 13, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A PATIENT LIFT SLING BY THE END USER'S DAUGHTER WHO STATED THAT THE BLUE STRAP ON THE SLING TORE IN HALF CAUSING THE END USER TO FALL BACKWARDS. THE END USER BROKE THEIR COLLARBONE. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Bone Fracture(s)
MAUDE report 21379525 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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