MAUDE Adverse Event Report: DRÄGERWERK AG & CO. KGAA EVITA V600; ANAESTHESIA AND PULMONARY VENTILATION SUPPORT INSTRUMENT

Model Number	8422300
Medical Device Problem Codes	No Display/Image (1183); Display or Visual Feedback Problem (1184); Device Difficult to Program or Calibrate (1496)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/19/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The investigation has just started; results will be provided in a follow-up report.
Event or Problem Description
It was reported that the screen was restarted during connection to the patient.The ventilation was working with no stop.No patient health consequences have been reported.
Additional Manufacturer Narrative
The affected evita v600 device was analyzed via provided information and the secured log files.The analysis of the logs shows no malfunction or restart on the day mentioned (02.19.2026).It could be identified that the error messages ¿device failure (14)¿ and the subsequent ¿alarm system failed¿ were issued one day before the reported event.Both alarms resulted from a temporary impairment of the internal hdbaset communication between the ecd and the ventilation unit.In such cases, display functions may be affected and the screen may turn black.In case of an internal failure of the display unit (ecd) and/or an impaired internal hdbaset communication between the ventilation unit and the ecd the alarm message "device failure (14)" will be raised.The display functions and operability of the ecd might be affected in case of an active "device failure (14)" alarm event depending on the technical root cause.If the internal hdbaset communication fails completely, the secondary alarm (piezo speaker) of the ventilation unit will sound.Safety relevant parameters as fio2, minute volume and airway pressure are displayed on the supplemental oled-display wherein the user can observe the ongoing ventilation.The device reacted as specified and needs to be checked according to the proper fitment of system cable and pba syscon ecd.Field quality data are monitored and assessed by responsible product quality board.The results of this investigation did not reveal any new risks which are not covered by the product risk management file.
Event or Problem Description
It was reported that the screen was restarted during connected to the patient.The ventilaton was working with no stop.No patient health consequences have been reported.

• Brand Name: EVITA V600
• Common Device Name: ANAESTHESIA AND PULMONARY VENTILATION SUPPORT INSTRUMENT
• Manufacturer (Section D): DRÄGERWERK AG & CO. KGAA; moislinger allee 53-55; lübeck ; GM
• Manufacturer (Section G): DRÄGERWERK AG & CO. KGAA; moislinger allee 53-55; lübeck 23558 ; GM 23558
• Manufacturer Contact: moislinger allee 53-55; lübeck 23558 ; 4518822868
• MDR Report Key: 24616173
• Report Number: 9611500-2026-00106
• Device Sequence Number: 15911179
• Product Code: CBK
• UDI-Device Identifier: 04048675548744
• UDI-Public: (01)04048675548744(11)250811(93)8422300-08
• Combination Product (Y/N): N
• Initial Reporter Country: SA
• PMA/510(K) Number: K222024
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/23/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 8422300
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 02/25/2026
• Supplement Date Received by Manufacturer: 03/27/2026
• Initial Report FDA Received Date: 03/17/2026
• Supplement Report FDA Received Date: 04/23/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 08/11/2025
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown