CHAIR PAD, 7x15, 14-DAY, 8FT 73030Recalls & reported problems
Securitas Healthcare LLC · CHAIR PAD, 7x15, 14-DAY, 8FT · Class 1
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 00840948102516), received between Feb 21, 2025 and Feb 21, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Labelling, Instructions for Use or Training Problem” (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
- Labelling, Instructions for Use or Training Problem1
Patient problems
- Head Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 21, 2025Labelling, Instructions for Use or Training Problem; Labelling, Instructions for Use or Training Problem
CHAIR ALARM PAD WEDGED INTO THE CHAIR AND DID NOT ALARM WHEN THE PATIENT GOT UP. THE PATIENT FELL AND SUSTAINED MULTIPLE RIGHT SIDED SUBDURAL HEMATOMAS.
Patient problems: Head Injury
MAUDE report 21440274 ↗
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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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