Single Patient Use HoverMatt HM39SPU-BRecalls & reported problems
Hovertech International · 39" Single Patient Use HoverMatt Breathable · Class 2
Data updated Oct 18, 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 00816299010800), received between Sep 30, 2019 and Sep 30, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Deflation 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.
Most reported problems
Device problems
- Deflation Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2019Deflation Problem
AT END OF CASE, PATIENT WAS TRANSFERRED FROM OR TABLE TO GURNEY VIA HOVERMAT WITH THE DIRECTION OF ANESTHESIOLOGIST. THERE WERE ALSO TWO RN'S AND ANESTHESIA RESIDENT HELPING WITH TRANSFER. THE HOVERMAT WAS INFLATED AND PATIENT WAS MOVED TO GURNEY. THE HOVERMAT WAS PRESSED TO DEFLATE AFTER TRANSFER TO GURNEY. AFTER DEFLATION, THE PATIENT WAS ON GURNEY BUT SLOWLY FELL TO HIS RIGHT SIDE OFF OF GURNEY. PATIENT WAS LIFTED BACK TO BED BY STAFF. DEVICE DEFLATED ASYMMETRICALLY CAUSING SLIDING.
Patient problems: Fall
MAUDE report 9134533 ↗
Other DEVICE, PATIENT TRANSFER, POWERED devices
- N/A HM39SPU-BStryker Sustainability Solutions, Inc. · DEVICE, PATIENT TRANSFER, POWERED1 recall0 reports
- HoverMatt HM34HSHovertech International · DEVICE, PATIENT TRANSFER, POWERED1 report
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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