Drive 13221LRecalls & reported problems
Drive Devilbiss Healthcare · Patient RoomSlings Product Description: Sling w/Cmde.Mesh,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 00822383103587), received between Sep 16, 2026 and Sep 16, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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 Split, Cut or Torn1
Patient problems
- Bone Fracture(s)1
- Hip Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 16, 2026Material Split, Cut or Torn
Drive Medical was notified of an incident involving a sling by a letter from an attorney. According to the information received, the end user was in a patient lift when the lift strap broke, resulting in a fall. As a consequence of the fall, the end user reportedly sustained a fractured elbow, fractured hip, and fractured pelvis. Drive Medical is currently investigating the incident, including attempting to inspect the device. An update will be filed if additional information becomes available.
Patient problems: Bone Fracture(s); Hip Fracture
MAUDE report 50791934 ↗
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- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 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.