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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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 ↗

Other Lift, Patient, Non-Ac-Powered devices

All Lift, Patient, Non-Ac-Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.