MERITS E60421YLMUBRecalls & reported problems
Merits Health Products CO., Ltd. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04714379292015), received between Feb 27, 2020 and Feb 27, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2020Physical Resistance/Sticking; Physical Resistance/Sticking
USER WAS RIDING FROM FIRST FLOOR TO THE SECOND WHEN APPROXIMATELY HALFWAY ALONG THE TRACK, THE PINION GEAR DISENGAGED FROM THE GEAR RACK ALLOWING THE LIFT TO SLIDE DOWNWARD. THE PINION GEAR RE-ARRANGED WITH THE GEAR RACK APPROXIMATELY HALF OF THE INITIAL TRAVEL BRINGING THE LIFT TO A SLOP. THE USER WAS SHAKEN BY THE MALFUNCTION AND SUFFERED MINOR BRUISING TO HIS ARM, NO HOSPITALIZATION WAS REQUIRED.
Patient problems: Bruise/Contusion
MAUDE report 9765465 ↗
Other Transport, Patient, Powered devices
- MERITS E60424YLMUBMerits Health Products CO., Ltd. · Transport, Patient, Powered1 recall0 reports
- XpeditionTM Powered Stair Chair (mid configuration) 625705550002Stryker Corporation · Transport, patient, powered26 reports
- XpeditionTM Powered Stair Chair (mid configuration) 6257Stryker Corporation · Transport, patient, powered18 reports
- XpeditionTM Powered Stair Chair (mid configuration) 625705550001Stryker Corporation · Transport, patient, powered9 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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