FDA Adverse Event Malfunction Summary report: N

CARESTATION 650

MDR report key: 22007883 · Received May 13, 2025

Report

Report Number
9710602-2025-00930
Event Type
Malfunction
Date Received
May 13, 2025
Date of Event
April 14, 2025
Report Date
May 13, 2025
Manufacturer
GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUXI)
Product Code
BSZ
UDI-DI
00840682103947
PMA / PMN Number
K151570
Removal / Correction Number
SEE H11
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
BIOMEDICAL ENGINEER
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HGE HEALTHCARE (GEHC) REPORTED A FIELD MODIFICATION FOR AN ISSUE THAT PREVENTS EFFECTIVE MECHANICAL VENTILATION IN VOLUME CONTROL VENTILATION (VCV) MODE PER 21 CFR 806 ON (B)(6) 2025. THE FDA RECALL NUMBERS ARE: Z-1624-2025, Z-1625-2025, Z-1626-2025, Z-1627-2025, Z-1628-2025, Z-1629-2025, Z-1630-2025, Z-1631-2025, Z-1632-2025, Z-1633-2025, Z-1634-2025, Z-1635-2025, Z-1636-2025, Z-1637-2025, Z-1638-2025. CUSTOMERS WERE SENT A LETTER EXPLAINING THE ISSUE AND PROVIDING INSTRUCTIONS FOR INSPECTING FOR EFFECTIVE VENTILATION IN VOLUME CONTROL VENTILATION (VCV) MODE. GEHC WILL CORRECT ALL DEVICES THAT FAIL THE VENTILATION SCREENING TEST AT NO COST. BLOCK A: NO PATIENT INVOLVEMENT. LEGAL MANUFACTURER: HCS MADISON - 3030 OHMEDA DR, USA MADISON, WI 53718.

Description of Event or Problem · 0

AS A RESULT OF AN INSPECTION THAT WAS COMPLETED AS PART OF THE CORRECTION INITIATED BY GE HEALTHCARE (GEHC) ON (B)(6) 2025, (GEHC FIELD ACTION NUMBER (B)(4)) THIS UNIT WAS IDENTIFIED AS HAVING AN ISSUE THAT PREVENTS EFFECTIVE MECHANICAL VENTILATION IN VOLUME CONTROL VENTILATION (VCV) MODE. THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2300887 CARESTATION 650 ANESTHESIA GAS MACHINE BSZ GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUXI) A1 NA 00840682103947

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown