HA90VRecalls & reported problems
Hill Laboratories CO. · Class 1
Data updated Oct 16, 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 00850058158082), received between Jul 21, 2025 and Jul 21, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Device Emits Odor” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device Emits Odor1
- Device Remains Activated1
- Thermal Decomposition of Device1
- Unintended Movement1
Patient problems
- 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.
InjuryJul 21, 2025Thermal Decomposition of Device; Device Emits Odor; Device Remains Activated; Unintended Movement; Thermal Decomposition of Device; Device Emits Odor; Device Remains Activated; Unintended Movement
FOLLOWING PATIENT TREATMENT, STAFF ATTEMPTED TO REPOSITION THE BED TO BRING INTO STANDARD PRONE POSITION. THE BED HAD NO ELECTRIC RESPONSE TO FOOT CONTROLS BUT CONTINUED TO TILT PATIENT INTO REVERSE TRENDELENBURG POSITION. STAFF WAS ABLE TO SECURE PATIENT AND ASSIST TO STANDING POSITION WITHOUT PATIENT INJURY HOWEVER THE PHYSICIAN WAS INJURED WHILE PROTECTING THE PATIENT FROM A FALL. THE MOTOR WAS NOTED TO CONTINUE TO RUN AND SMELLED OF BURNING ELECTRIC PARTS.
Patient problems: Unspecified Tissue Injury
MAUDE report 22556503 ↗
Other Table, Powered devices
- Trademark Elevating Table E9012-LPivotal Health Solutions, Inc. · Table, Powered1 recall3 reports
- SARA COMBILIZER APA1000-USArjohuntleigh AB · Table, 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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