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Recalls → Z-0132-2027
Class I Recall · Z-0132-2027 Report Date: 2026-10-28 · Status: Ongoing

Ventec Life Systems, Inc. — Medical Devices Recall

Product Description: V+ Pro Emergency, Model Number: PRT-01201-000, Package PN:PRT-01173-000,PRT-01222-000. used for ventilatory support.
Reason for Recall: Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
Distribution Pattern: Distribution US nationwide including Puerto Rico.
View Linked Facility Profile (FEI FEI-DB14376C) → Verify on openFDA ↗