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VentStar Coax (P) MP00379Recalls & reported problems

Drägerwerk AG & Co. KGaA · Class 1

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. 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-1451-2023 · Root cause: Process control · FDA record ↗

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

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

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.