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VentStar Anesthesia (N) 180 MP00333Recalls & reported problems

Drägerwerk AG & Co. KGaA · Class 1

Data updated Oct 16, 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 16, 2026.

Recalls naming this device

  1. Apr 17, 2023Terminated

    Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

    Z-1447-2023 · Root cause: Process control · Recall details · FDA record ↗

Other Circuit, Breathing (W Connector, Adaptor, Y Piece) devices

All Circuit, Breathing (W Connector, Adaptor, Y Piece) devices →

Sources and updates

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