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Suction Valve EN10232Recalls & reported problems

GA Health Company Limited · Class 2

Data updated Oct 13, 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Nov 3, 2020Terminated

    Suction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure

    Z-0642-2021 · Root cause: Process control · FDA record ↗

Other Endoscopic Irrigation/Suction System devices

All Endoscopic Irrigation/Suction System devices →

Sources and updates

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