Maxi Sky 2 MS110Recalls & reported problems
Arjohuntleigh AB · Maxi Sky 2, 4F CSTAT - Ceiling Lift - Safe working load of 600 lb / 272 kg. · Class 1
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 05056097356815), received between Aug 25, 2022 and Sep 15, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Detachment of Device or Device Component
The customer representative contacted Arjo and reported that the spreader bar had detached from the Maxi Sky 2 lift. No patient was involved at the time of the event, and no injuries were reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50771021 ↗MalfunctionFeb 28, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
FOLLOWING THE INFORMATION REPORTED, THE MAXI SKY 2 SPREADER BAR DETACHED DURING THE PREPARATION OF THE LIFT FOR PATIENT TRANSFER (DURING THE LOWERING OF THE LIFT). AS A CONSEQUENCE, THE SPREADER BAR FELL ON THE RESIDENT, BUT ITS WEIGHT WAS HELD BY THE STAFF WHICH PREVENTED AN IMPACT. NO INJURY WAS REPORTED. AFTER THE EVENT, AN ARJO REPRESENTATIVE CONDUCTED THE DEVICE INSPECTION AT THE CUSTOMER'S SITE. ACCORDING TO THE SERVICE TECHNICIAN, THE CEILING LIFT WAS OPERATING CORRECTLY AND THE SPREADER BAR QUICK-CONNECT ATTACHMENT COMPONENTS (COVER AND LATCH) HAD NO SIGNS OF DAMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16450987 ↗MalfunctionOct 6, 2022Detachment of Device or Device Component; Detachment of Device or Device Component
ARJO WAS INFORMED ABOUT THE INCIDENT WITH THE MAXI SKY 2 CEILING LIFT INVOLVEMENT. FOLLOWING THE INFORMATION PROVIDED, THE CAREGIVERS WERE POSITIONING THE DEVICE OVER A RESIDENT WHO WAS IN A BED. WHEN ONE OF THE CAREGIVERS ATTEMPTED TO ATTACH A SLING TO THE LIFT'S SPREADER BAR LUGS, THE SPREADER BAR DISCONNECTED FROM THE LIFTING STRAP. THE DETACHED PART LANDED ON THE RESIDENT'S ABDOMEN BUT DID NOT CAUSE ANY INJURIES. AFTER THE EVENT, AN ARJO REPRESENTATIVE WAS CALLED TO INSPECT THE DEVICE. THE SERVICE TECHNICIAN DID NOT FIND ANY DEVICE MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15549429 ↗MalfunctionAug 25, 2022Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A RESIDENT TRANSFER FROM A WHEELCHAIR TO A BED, THE SPREADER BAR OF THE MAXI SKY 2 CEILING LIFT DISCONNECTED FROM THE LIFTING STRAP. AT THE TIME OF THE INCIDENT, THE RESIDENT WAS ABOVE THE BED AND WAS DROPPED ON THE BED FROM A HEIGHT OF ABOUT 5 CM. THE RESIDENT DID NOT SUSTAIN ANY INJURIES. AFTER THE EVENT AN ARJO REPRESENTATIVE CONDUCTED THE DEVICE INSPECTION AT THE CUSTOMER'S SITE. ACCORDING TO THE SERVICE TECHNICIAN, THE CEILING LIFT WAS OPERATING CORRECTLY AND THE SPREADER BAR AND THE CLIP OF THE QUICK-CONNECT SPREADER BAR MECHANISM HAD NO DAMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15291573 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.