Feb

1998

Venturi Ventilator Class II 22 units

Venturi Ventilator, used to provide a software that continouslyadapts to the patient’s changing breathing demands and assures
ventilation at the lowest pressure. The display monitor provides
pertient patient parameters and waveforms. Recall #Z-802-9.

REASON

Display monitor may go blank due to faulty inverter.

CODE

Serial numbers: 970192, 970190, 970154, 970164, 970169, 970172,
970138, 970161, 970163, 970185, 970176, 970174, 970173, 970166,
970184, 970186, 970199, 970175, 970171, 970170, 970168, 970165.

MANUFACTURER

Cardiopulmonary Corporation, Milford, Connecticut.

RECALLED BY

Manufacturer, by letter on February 23, 1998, followed by visit.
Firm-initiated recall complete.

DISTRIBUTION

England.

QUANTITY

22 units were distributed.

About the author

Amy Sellers

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

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Venturi Ventilator Class II 22 units

Amy Sellers

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