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Terumo® Advanced Perfusion System 1 217390Recalls & reported problems

Terumo Cardiovascular Systems Corporation · Ultrasonic couplant used to facilitate the transmission of sound energy between the level sensor and the reservoir. · Class 2

All models of Terumo Advanced Perfusion System 1 (31)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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.

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.

Recalls naming this device

  1. Feb 20, 2017Class IITerminated

    Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and Level Sensor Gel Pads due to non-compliant labeling because the product expiration date is displayed in a format that may not be recognizable to all users.

    Z-1459-2017 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Console, Heart-Lung Machine, Cardiopulmonary Bypass devices

All Console, Heart-Lung Machine, Cardiopulmonary Bypass devices →

Sources and updates

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