EZ Smart Lift L600PS-02Recalls & reported problems
EZ Way, Inc. · 600 lb. Smart Lift® with scale, Standard · Class 1
Data updated Oct 18, 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 00848914000019), received between Jun 7, 2024 and May 7, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
- Labelling, Instructions for Use or Training Problem1
- Premature Separation1
- Use of Device Problem1
Patient problems
- Bone Fracture(s)1
- Head Injury1
- Limb Fracture1
- Multiple Fractures1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2026Insufficient Device Problem Information
TRANSFERRING RESIDENT FROM WHEELCHAIR TO BED. RESIDENT WAS UP IN AIR OFF OF CHAIR. THE CNAS PULLED THE CHAIR OUT FROM UNDER RESIDENT AND WERE GETTING READY TO TURN. THEY HEARD A SNAP SOUND AND THE RESIDENT FELL TO THE FLOOR. THE RESIDENT'S RIGHT SIDE WAS OUT OF SLING AND RESIDENT HIT HEAD ON FLOOR. RESIDENT HAD BROKEN A FEMUR, BROKEN COLLAR BONE, AND BROKEN NECK. THE RESIDENT HAD A SUBDURAL HEMATOMA.
Patient problems: Bone Fracture(s); Head Injury; Multiple Fractures
MAUDE report 25116643 ↗InjuryJun 7, 2024Labelling, Instructions for Use or Training Problem; Use of Device Problem; Premature Separation; Labelling, Instructions for Use or Training Problem; Use of Device Problem; Premature Separation
2 CAREGIVERS TRANSFERRING RESIDENT FROM BED TO CHAIR AND RESIDENT FELL. CARISSA SAID ONE OF THE HARNESS STRAPS CAME OFF THE STAND. THE RESIDENT FELL AND HAD A FRACTURED FEMUR.
Patient problems: Limb Fracture
MAUDE report 19485139 ↗
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- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- 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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