EZ Smart Lift L500PN-02Recalls & reported problems
EZ Way, Inc. · 500 lb. Smart Lift® without scale, Standard · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 2
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00848914000040), received between Aug 8, 2024 and May 18, 2026 — classified as 2 deaths, 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (2 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. 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
- Improper or Incorrect Procedure or Method2
- Use of Device Problem2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Bone Fracture(s)2
- Fall1
- Hip Fracture1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
DeathMay 18, 2026Use of Device Problem; Improper or Incorrect Procedure or Method
STAFF WAS GOING FROM BED TO WHEELCHAIR. THEY HAD A SIDE ENTRANCE AND THE LIFT TIPPED DURING PROCESS. THE RESIDENT FELL ON FLOOR STILL IN THE SLING. THEY HAD TO UNHOOK THE SLING TO GET RESIDENT OUT AND BACK UP. THE RESIDENT BROKE HER HIP.
Patient problems: Bone Fracture(s); Hip Fracture
MAUDE report 25203772 ↗DeathMay 14, 2026Use of Device Problem; Improper or Incorrect Procedure or Method
CNA WAS ON EACH SIDE OF BED, HOOKING UP STRAPS TO THE LIFT. THE CNA ON THE SIDE OF THE BED WITH THE MACHINE HOOKED UP A LOOP TO THE LIFT AND MOVED TO THE OTHER SIDE OF THE BED. WHILE MOVING TO THE OTHER SIDE, THE CNA WAS PICKING THINGS UP AND MOVING THINGS AND ONE OF THE LEG LOOPS DID NOT GET HOOKED UP TO THE MACHINE. WHEN THE RESIDENT WAS LIFTED OFF THE BED, SHE SLID OUT OF THE SLING. THE RESIDENT DIED THE NEXT DAY. (B)(6) SAID THE LIFT WAS NOT AT FAULT AND THIS WAS USER ERROR.
Patient problems: Fall
MAUDE report 25173528 ↗InjuryAug 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
FACILITY STATED: 2 CNAS WERE TRANSFERRING RESIDENT FROM COMMODE TO BED. THE UPPER RIGHT-HAND LOOP BY SHOULDER CAME OFF OF HANGER BAR AND RESIDENT FELL TO THE FLOOR. (B)(6) SAID THE RESIDENT WAS A VERY TOP-HEAVY PERSON. DURING THE TRANSFER, THE RESIDENT CROSSED HER HANDS AND KEPT THEM TO HERSELF. SHE WAS RIDING IN THE SLING AS DIRECTED. STAFF NOTICED A GREEN CAP CAME OFF THE HANGER BAR. THEY SAID THE GREEN CAP WAS ON THE HANGER BAR BEFORE THE TRANSFER. (B)(6) SAID THEY TRIED TO RE-ENACT THE INCIDENT, BUT THEY DON'T KNOW EXACTLY HOW IT HAPPENED. MAYBE THE RESIDENT'S BOTTOM BRUSHED THE BED OR MAYBE THE RESIDENT SHIFTED HER WEIGHT. POSSIBLY SLING WAS OFF SLIGHTLY AND WASN'T POSITIONED BEFORE MOVING THE RESIDENT. (B)(6) ALSO QUESTIONED IF THE SLING WAS POSITIONED TOO FAR UP ON RESIDENT'S BACK THE RESIDENT WAS LIFE FLIGHTED TO THE HOSPITAL. LAST KNOWN STATUS IS PATIENT WAS IN ICU. NO KNOWLEDGE OF ANY SURGERY AS OF 12:30PM ON (B)(6) 2024.
Patient problems: Bone Fracture(s)
MAUDE report 19939277 ↗
Other Lift, Patient, Non-Ac-Powered devices
- MEDLINE MDS88200DMedline Industries, Inc. · Lift, patient, non-ac-powered108 reports
- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- Likorall™ overhead lift 3123001Liko AB · Lift, patient, non-ac-powered1 recall1 death32 reports
- 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
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page