Liko Solo HighBack Sling™, Mod. 25 3525915Recalls & reported problems
Liko AB · Patient lifting system divided leg sling · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887761983403), received between Mar 7, 2024 and Mar 19, 2025 — classified as 1 injury, 1 malfunction.
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Material Split, Cut or Torn1
Patient problems
- Bone Fracture(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
THE CUSTOMER REPORTED THAT THE LIKO SOLO HIGH BACK SLING BROKE DURING A PATIENT TRANSFER. IT WAS NOTED THAT THE PATIENT HAD FALLEN OUT OF BED AND NEEDED TO BE LIFTED BACK INTO BED AS THEY COULD NOT STAND ON THEIR LEGS. THE STAFF PLACED THE SLING AND CONNECTED IT TO THE LIFT, HOWEVER, WHEN THE TRANSFER WAS INITIATED, A LOUD BANG WAS HEARD AS THE SLING HAD BROKEN AT THE SEAMS. FORTUNATELY, THE PATIENT WAS NOT TOO HIGH ABOVE THE FLOOR, HOWEVER, DUE TO THEIR WEIGHT, THEY FELL HARD ON THEIR SHOULDER REGION. THE PATIENT SUBSEQUENTLY HAD AN X-RAY OR CT SCAN OF THEIR SHOULDER (REPORTER COULD NOT REMEMBER), WHICH SHOWED A SMALL FRACTURE THAT HAD TO BE TREATED CONSERVATIVELY.
Patient problems: Bone Fracture(s)
MAUDE report 21642687 ↗MalfunctionMar 7, 2024
PATIENT WAS BEING LIFTED FROM THE BED TO THE CHAIR WITH THE CEILING LIFT AND GREEN SLING. WHILE THE PATIENT WAS IN THE AIR, THERE WAS LOUD POPPING COMING FROM THE SLING. THE PATIENT WAS IMMEDIATELY LOWERED, AND THE SLING WAS REMOVED. SOME STITCHES IN THE FABRIC APPEARED TO BE BROKEN. THE SLING USED WAS RATED FOR UP TO 440LB. NO PATIENT HARM, NO DAMAGE TO LIFT EQUIPMENT. GRABBED NEW SLING AND IT WORKED AS EXPECTED. MANUFACTURER RESPONSE FOR SLING, SOLO HIGHBACK SLING (PER SITE REPORTER). THIS WAS REPORTED TO THE VENDOR ON FRIDAY, 10/20/2023. ON MONDAY 10/23/2023 THE PO # THAT THE SLING WAS PURCHASED WAS SENT TO THE VENDOR ALONG WITH A REQUEST THAT THEY SEND A CALL TAG FOR THE REVIEW OF THE PRODUCT. THE VENDOR HAS NOT REPLIED BACK. THE VENDOR WAS EMAILED AGAIN TODAY 10/26/2023 AND THEY HAVE NOT YET REPLIED BACK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18855875 ↗
Other Lift, patient, non-ac-powered devices
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- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
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- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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