ClearanceBrief
Recall Z-0108-2022 ยท CBK Ventilator, Continuous, Facility Use

Draeger Medical, Inc.

Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the ventilation of adult,pediatric and neonatal patients. Catalog Number: 8416400

DateSep 10, 2021
StatusOpen, Classified
ReasonSoftware 2.51 and Lower with Installed CO2 Measurement Option, may result in Restart of the Ventilator, brief cessation of ventilation can occur and loss of PEEP for approx. 8 seconds
Root causeSoftware design
ActionDrager issued Urgent Medical Device Recall letter on 9/10/21 via FedEx with tracking (confirmation of delivery). Letter states reason for recall, health risk and action to take: The release of a corrected software is expected to be available in Q4 of 2021. Once the software is available, your local Drger Service representative will contact you to arrange a date for the software update to be performed free of charge. According to our records, at least one of the mentioned affected devices has been shipped to your facility. Please ensure that all users of the above-mentioned products and other
Quantity6,797 units
DistributionUS Nationwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K093633INFINITY ACUTE CARE SYSTEM WORKSTATION CRITICAL CARE
Draegerwerk AG & CO Kgaa, Mar 30, 2010