imagiQ imagiQ3 LegacyRecalls & reported problems
Stille AB · TABLE, OPERATINGROOM, ELECTRICAL · Class 1
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 07332339238179), received between Aug 25, 2025 and Aug 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation, Positioning or Separation 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
- Activation, Positioning or Separation Problem1
- Key or Button Unresponsive/not Working1
- Mechanical 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.
MalfunctionAug 25, 2025Mechanical Problem; Activation, Positioning or Separation Problem; Key or Button Unresponsive/not Working; Mechanical Problem; Activation, Positioning or Separation Problem; Key or Button Unresponsive/not Working
B5: DESCRIPTION OF EVENT: DURING OR AT END OF A PROCEDURE, (B)(6) 2025, THE STANDARD TRENDELENBURG MOVEMENT OF THE TABLE STOPPED WORKING UNEXPECTEDLY DUE TO A LOOSENED INTERNAL SCREW. PLEASE NOTE THAT THE REVERSE TRENDELENBURG AND EMERGENCY TRENDELENBURG FUNCTIONS REMAINED FULLY OPERATIONAL. ALTHOUGH NO PATIENT HARM OCCURRED, WE BELIEVE THIS MALFUNCTION COULD POTENTIALLY LEAD TO A SERIOUS INJURY IF IT WERE TO OCCUR DURING A CRITICAL SURGICAL PROCEDURE. MORE CLOSELY, THE END USER DID NOT KNOW THAT THE MALFUNCTION DEPENDED ON THE LOOSEN SCREW, BUT WE UNDERSTOOD IT WHEN STILLE'S SERVICE ENGINEER CAME ON SITE 17 JUNE.
Patient problems: Fall
MAUDE report 22888431 ↗
Other Table, Operating-Room, Electrical devices
- NA 72203299Smith & Nephew, Inc. · TABLE, OPERATING-ROOM, ELECTRICAL298 reports
- TS 7000 1723633Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall22 reports
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall9 reports
- Head-Positioning accessories 1739994Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall1 report
- TS 7500 2067886Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall0 reports
- TS 7500 4091000Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- TS 7500 1717021Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 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 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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