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Terumo® Advanced Perfusion System 1 5791Recalls & reported problems

Terumo Cardiovascular Systems Corporation · The air sensor is a non-invasive, ultrasonic sensor that can detect air bubbles in the perfusion circuit. This is the 1/4"x3/32" sensor. Includes cable and holder. · 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. Aug 25, 2020Class IITerminated

    Internal testing at the supplier, revealed that a crimped wire was placed into an air bubble detector (ABD) sensor connector backwards, preventing the crimped wire from locking into the mating wire connector. This intermittent connection may result in false air bubble alarms.

    Z-2961-2020 · Root cause: Employee error · Recall details · FDA record ↗

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Sources and updates

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