FDA Device Intelligence
HomeO-Two Medical Technologies Inc › CAREvent MRI

CAREvent MRI

O-Two Medical Technologies Inc · Model 01CV7000 · UDI-DI 07540195030183

BTL Prescription
1
510(k) clearances
4,749
Adverse events (34 deaths)
29
Recalls
47
Facilities

Description

CAREvent MRI is pneumatically powered, time/volume cycled, intermittent positive pressure patient ventilators specifically designed for use by trained personnel in the pre-hospital, hospital, interhospital and air ambulance environments. It has independent controls for minute volume and frequency that provide a comprehensive range of 12 ventilation frequencies and 12 minute-volume settings. This provides a possible 144 combinations of delivered tidal volume and respiratory rate. The various modes of operation of the ventilators support the resuscitation and transportation of a wide range of patients (from infants to adults). The CAREvent MRI contains no ferrous metals and is suitable for use in a three-Tesla MRI environment.

Recalls

DateFirmReason
2024-12-10Mercury Enterprises, Inc. dba Mercury MedicalGas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and
2024-08-30Mercury Enterprises, Inc. dba Mercury MedicalManual resuscitator circuit flow controller may come apart due to a missing manufacturing step.
2024-05-31Smiths Medical ASD Inc.Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P310 ventilators impacting the activ
2024-05-31Smiths Medical ASD Inc.There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.
2024-05-31Smiths Medical ASD Inc.Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P310 ventilators impacting the activ
2024-05-31Smiths Medical ASD Inc.There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.
2024-02-07Smiths Medical ASD Inc.When a paraPAC plus ventilator is switched to the operating mode of VENTILATE, the ventilator may intermittently provide continuous positive gas flow instead of the intended cyclin
2024-02-07Smiths Medical ASD Inc.When a paraPAC plus ventilator is switched to the operating mode of VENTILATE, the ventilator may intermittently provide continuous positive gas flow instead of the intended cyclin
2021-07-15Smiths Medical ASD Inc.Two devices were labeled with the same serial number
2020-06-26Precision Valve & Automation,IncWhile operating the machine in "Run" mode an unexcepted event may occur during the error-checking for stepper movements and pressure values. The result of this event is a false ala

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.