MERITS P325 30200589Recalls & reported problems
Merits Health Products CO., Ltd. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04714379292305), received between Apr 8, 2021 and Apr 8, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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.
Most reported problems
Device problems
- Fracture1
Patient problems
- Cellulitis1
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 8, 2021Fracture; Fracture
THE SEAT POST OF AN END USER'S POWER CHAIR HAS BROKEN OFF COMPLETELY WHILE THE END USER WAS OCCUPYING IT AND THE END USER WAS INJURED. IT WAS LATER REPORTED TO US (24MAR2021) THAT SHE HAD BEEN HOSPITALIZED AND HAD TO HAVE SURGERY ON HER EYELID DUE TO CELLULITIS.
Patient problems: Cellulitis; Unspecified Tissue Injury
MAUDE report 11636812 ↗
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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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