TS 7500 1854086Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · TruSystem 7500 Hybrid (SC) · Class 2
Data updated Oct 13, 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
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
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. How this data works · Data updated Oct 13, 2026.
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-1418-2025 · Root cause: Software design · FDA record ↗
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 1730731Baxter 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
- TS 7500 1854088Baxter 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 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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