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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

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: 1 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: 2 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

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

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Sources and updates

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