TS 7500 1909793Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · OR table top U26 H V · Class 1
All models of TS 7500 (16)
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 00887761974036), received between Jul 23, 2025 and Jul 23, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 Dislodged or Dislocated1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 23, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED, THE HEAD PLATE OF AN OR TABLETOP U26 H V COLLAPSED. DURING AN UNSPECIFIED BREAST PROCEDURE AND JUST BEFORE WAKING THE PATIENT FROM ANESTHESIA, THE HEAD PLATE OF THE TRUSYSTEM 7500 OPERATING TABLE COLLAPSED TO THE FLOOR WITHOUT WARNING. THE PATIENT¿S HEAD DROPPED RAPIDLY BACKWARDS IN HYPEREXTENSION. ONE OF THE HOSPITAL EMPLOYEES MANAGED TO GRAB THE PATIENT¿S HEAD BEFORE IT DROPPED FURTHER DOWN AND IMMEDIATELY STRAIGHTENED THE NECK TO ITS NATURAL POSITION. THE CUSTOMER STATED THAT THE OPERATION WENT WELL AND INITIALLY THE INCIDENT WAS NOT CONSIDERED TO HAVE HAD ANY IMPACT ON THE PATIENT. THE INCIDENT WAS RECORDED, AND THE PATIENT WAS INFORMED BEFORE BEING DISCHARGED. THE PATIENT DID NOT HAVE ANY SYMPTOMS OR DISCOMFORT AT THAT TIME. THREE DAYS AFTER THE INCIDENT, THE PATIENT REPORTEDLY SOUGHT MEDICAL CARE IN THEIR HOMETOWN DUE TO PAIN AND DISCOMFORT IN THE BACK OF THEIR NECK, AND WHIPLASH SYMPTOMS. THE PATIENT WAS ADVISED TO WEAR A NECK COLLAR AND TAKE UNREPORTED PAIN MEDICATIONS. IT WAS ALSO NOTED THAT THE PATIENT UNDERWENT AN MRI SCAN IN A DIFFERENT HEALTHCARE FACILITY AND THE RESULTS WERE NOT PROVIDED. AN INSPECTION PERFORMED BY THE HOSPITAL¿S TECHNICIANS NOTED THA
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 22575876 ↗
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
- TS 7500 1717021Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- TS 7500 4091000Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- ALLEN 107003Hill-Rom, Inc. · 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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