TS 7000 1604788Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761967526), received between Nov 12, 2025 and Apr 14, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (3 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Sep 19, 2024Open, Classified

   The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

   Z-0210-2025 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 14, 2026Unintended Movement; Device Fell

  BAXTER RECEIVED A REPORT THAT OPERATING TABLE TRUSYSTEM 7000 HAD AN UNINTENDED MOVEMENT WHEN RAISING THE TABLE. IT WAS NOTED WHEN RESETTING THE TABLE, IT DROPPED TO THE FLOOR. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24872612 ↗
• MalfunctionDec 1, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 MOVED WITH THE FLOOR LOCKS ON AND WITHOUT REMOTE GUIDANCE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23681406 ↗
• MalfunctionNov 25, 2025Mechanical Jam; Key or Button Unresponsive/not Working; Mechanical Jam; Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT DURING A CASE, THE TRUSYSTEM 7000 TABLE WAS MOVING UP, THE TABLE MADE A LOUD SOUND AND NO FUNCTIONS WERE AVAILALE AFTER THAT. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23645758 ↗
• MalfunctionNov 12, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRU SYSTEM 7000 U HEAD SECTION WILL NOT STAY IN PLACE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23538689 ↗