TS 7500 1730720Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Mobile column TruSystem 7500 U · Class 2
All models of TS 7500 (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761974388), received between Nov 10, 2025 and Nov 10, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Key or Button Unresponsive/not Working” (1 report).
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.
Reports received per month
Recalls naming this device
- 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 ↗
Most reported problems
Device problems
- Key or Button Unresponsive/not Working1
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.
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 ↗
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 1730731Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1717020Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1730732Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- NA 7265300Ge Healthcare(Tianjin) Company Limited · Table, radiologic1 recall0 reports
- NA 6265300-20GE Medical Systems, L.L.C. · 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 · each recall links to the FDA recall notice
- 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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