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TS 7500 1854087Recalls & reported problems

Baxter Medical Systems GmbH + Co. KG · TruSystem 7500 Hybrid Plus (FC) · Class 1

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
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

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

Other TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page