731 Series Ventilators running software version 05.20.00 The devices in the ZOLL ventilator are indicated for use in the management of infant through adult patients weighing ;:: 5 kg with acute or chronic respiratory failure or during resuscitation by providing continuous positive-pressure ventilation. They are appropriate for use in hospitals, outside the hospital, during transport and in severe environments where they may be exposed to rain, dust, rough handling, and extremes in temperature and humidity. With an appropriate third-party filter in place, they may be operated in environments where chemical and/or biological toxins are present. When marked with an MRI conditional label, they are suitable for use in an MRI environment with appropriate precautions. The ventilators are intended for use by skilled care providers with knowledge of mechanical ventilation, emergency medical services (EMS) personnel with a basic knowledge of mechanical ventilation, and by first responders under the direction of skilled medical care providers. The EMV+ and Eagle II (with and without MRI label) have a full range of ventilation modes (AC, SIMV with or without PS, CPAP with or without PS with PPC or NPPV-PPV). The AEV provides specific modes consistent with pre-hospital care provider s operating procedures (AC, CPAP with PS and NPPV-PPV). The ZOLL ventilators are a small, extremely durable, full-featured portable mechanical ventilator designed to operate in hospitals or severe and under-resourced environments. It can be used in prehospital (ALS, ATLS, ACLS), field hospitals, and hospital settings. Easy to-use, durable,
FDA Recall Z-0812-2018 · Posted None
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Recalling FirmZOLL Medical Corporation
Recall StatusTerminated
Product CodeCBK
Date Initiated2017-06-30
Date Terminated2018-10-09
Product Quantity46
Reason for Recall
A software anomaly in the 731 software version 05/20/00, was identified, which can lead to a user inadvertently changing device settings.
Firm Action
On June 30, 2017 an urgent recall letter was mailed to customers with the following instructions:
Customers who have affected devices should immediately take the following steps: (1) Alert all users of 731 Ventilator models to this problem.
(2) Direct users to always verify device parameters after selecting the device Confirm button.
(3) Contact ZOLL's Technical Service Department or your local ZOLL Service Provider to schedule a software update for affected devices
Our 24/7 technical support numbers 1(800) 348-9011 or +l (978) 421- 9460 are available to assist users with any aspect of this notice.
Root Cause
Under Investigation by firm
Distribution Pattern
Outside US
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
K111473UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATORImpact Instrumentation, Inc. · 2012-02-16K103318UNI-VENT 731 SERIES MODEL EMV+ PORTABLE CRITICAL CARE VENTILATORImpact Instrumentation, Inc. · 2011-04-07K091238UNI-VENT-731 SERIES VENTILATORS, MODEL 731EMV+Impact Instrumentation, Inc. · 2009-08-13K071526UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMVImpact Instrumentation, Inc. · 2008-12-10
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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