TRUMPF MEDICAL 1717023Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Hillrom™ Mobile column TruSystem 7500 · Class 2
All models of TRUMPF MEDICAL (11)
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 00887761993150), received between Sep 29, 2025 and Sep 29, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Fell” (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
- Device Fell1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2025Device Fell; Device Fell
BAXTER RECEIVED A REPORT STATING THAT AFTER THE PATIENT TRANSFER TO THE CARBON FLOATLINE TABLETOP, TRUSYSTEM 7500 MAIN LIFT OF THE SURGICAL TABLE DROPPED DOWN. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23168637 ↗
Other Table, radiologic devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Radiologic2 recalls6 reports
- NA 6265300GE Medical Systems, L.L.C. · Table, radiologic2 recalls0 reports
- PST500 4080300Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall4 reports
- TS 7500 1730720Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall1 report
- TS 7500 1854086Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1730732Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- NA 6265300-20GE Medical Systems, L.L.C. · Table, radiologic1 recall0 reports
- TS 7000 1604786Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page