TS 7500Recalls & reported problems across all models

We found 16 models of TS 7500 by Baxter Medical Systems GmbH + Co. KG in the FDA's device registry (GUDID). Together they are named in 4 adverse event reports in the FDA's MAUDE database, received between Jul 23, 2025 and Nov 10, 2025 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

14 FDA recall records name at least one of these models by its device identifier, 14 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

TS 7500 recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1422-2025 · Root cause: Software design · Recall details · FDA record ↗

2. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1421-2025 · Root cause: Software design · Recall details · FDA record ↗

3. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1420-2025 · Root cause: Software design · Recall details · FDA record ↗

4. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1419-2025 · Root cause: Software design · Recall details · FDA record ↗

5. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1418-2025 · Root cause: Software design · Recall details · FDA record ↗

6. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1417-2025 · Root cause: Software design · Recall details · FDA record ↗

7. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1416-2025 · Root cause: Software design · Recall details · FDA record ↗

8. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1415-2025 · Root cause: Software design · Recall details · FDA record ↗

9. Feb 25, 2025Open, Classified

   There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

   Z-1414-2025 · Root cause: Software design · Recall details · FDA record ↗

10. Feb 25, 2025Open, Classified

    There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

    Z-1413-2025 · Root cause: Software design · Recall details · FDA record ↗

11. Feb 25, 2025Open, Classified

    There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

    Z-1412-2025 · Root cause: Software design · Recall details · FDA record ↗

12. Feb 25, 2025Open, Classified

    There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

    Z-1411-2025 · Root cause: Software design · Recall details · FDA record ↗

13. Feb 25, 2025Open, Classified

    There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

    Z-1410-2025 · Root cause: Software design · Recall details · FDA record ↗

14. Feb 25, 2025Open, Classified

    There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

    Z-1409-2025 · Root cause: Software design · Recall details · FDA record ↗

Most reported TS 7500 problems

TS 7500 models

16 models, most reported first. Each model has its own page with its reports, recalls and device details.

• TS 7500 1730720

  Table, radiologic
  1 recall1 report
• TS 7500 1717023

  TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
  1 recall1 report
• TS 7500 4091000

  TABLE, OPERATING-ROOM, ELECTRICAL
  1 recall0 reports
• TS 7500 2067886

  TABLE, OPERATING-ROOM, ELECTRICAL
  1 recall0 reports
• TS 7500 1854088

  Table, radiologic
  1 recall0 reports
• TS 7500 1854087

  TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
  1 recall0 reports
• TS 7500 1854086

  Table, radiologic
  1 recall0 reports
• TS 7500 1854085

  TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
  1 recall0 reports
• TS 7500 1773204

  Table, radiologic
  1 recall0 reports
• TS 7500 1730732

  Table, radiologic
  1 recall0 reports
• TS 7500 1730731

  Table, radiologic
  1 recall0 reports
• TS 7500 1717021

  TABLE, OPERATING-ROOM, ELECTRICAL
  1 recall0 reports
• TS 7500 1717020

  Table, radiologic
  1 recall0 reports
• TS 7500 1704695

  TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
  1 recall0 reports
• TS 7500 2064888

  Table, radiologic
  1 report
• TS 7500 1909793

  TABLE, OPERATING-ROOM, ELECTRICAL
  1 report

Recent TS 7500 adverse event reports

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

• MalfunctionNov 10, 2025Key or Button Unresponsive/not Working; Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT TRUSYSTEM 7500 U MOBILE COLUMN HAD NO FUNCTIONS. THE TABLE WAS LOCATED AT THE ACCOUNT AND OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23511614 ↗
• MalfunctionAug 22, 2025Device Fell; Device Fell

  BAXTER RECEIVED A REPORT STATING THAT DURING THE OPERATION, TRUSYSTEM 7500 TABLE TOP COLLAPSED WITHOUT ANY INPUT FROM THE NURSING STAFF. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22874958 ↗
• MalfunctionJul 25, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLETOP MIDDLE BACK SECTION WAS MOVING DOWN WITHOUT ANY USER INPUT. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22612578 ↗
• 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 Baxter Medical Systems GmbH + Co. KG products

• TRUMPF MEDICAL11 models · 78 reports
• TS 70003 models · 26 reports · 1 recall
• iLED7 Surgical Light6 models · 11 reports · 1 recall
• TL 5000/3000 – Surgical Light2 models · 2 reports · 1 recall
• VidiaPort3 models · 1 reports · 1 recall
• iLED5 models · 41 reports