FDA Adverse Event Malfunction Summary report: N

SERVO-I BASE UNIT

MDR report key: 19095329 · Received April 12, 2024

Report

Report Number
8010042-2024-00608
Event Type
Malfunction
Date Received
April 12, 2024
Date of Event
March 12, 2024
Report Date
April 12, 2024
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
PMA / PMN Number
K123149
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

ON-SITE INVESTIGATION WAS PERFORMED BY OUR FIELD SERVICE ENGINEER. ACCORDING TO RECEIVED INFORMATION, SUPPORT ARM 176 WAS BROKEN AT JOINT. THE SUPPORT ARM SERVES TO RELIEVE THE PATIENT FROM THE WEIGHT OF THE TUBING SYSTEM. IT IS WORTH MENTIONING THAT CUSTOMER IS OBLIGED TO FOLLOW THE INSTALLATION INSTRUCTIONS DELIVERED TOGETHER WITH THE DEVICE. FOR EXAMPLE, ACCORDING TO INSTALLATION INSTRUCTIONS FOR THE SUPPORT ARM 177 IN THE SPECIFICATION OF THE MAXIMUM CAPACITY, IT IS STATED HOW MANY KILOGRAMS CAN BE LOADED DEPENDING ON THE ANGLE OF USE OF THE ACCESSORIES (MAX. APPROX. 3 KG). WHEN MOVING THE SUPPORT ARM OR CHANGING POSITION, THE PATIENT CONNECTION SHOULD BE OBSERVED TO SEE THAT NO PULLING OR OTHER MOVEMENT OCCURS. THE CAUSE OF THE CLAIMED ISSUE IN THIS CUSTOMER PRODUCT COMPLAINT HAS BEEN DETERMINED. THE ISSUE WAS RELATED TO DEFECTIVE JOINTS OF SUPPORT ARM. THE UDI INFORMATION IS NOT AVAILABLE SINCE THE DEVICE WAS MANUFACTURED BEFORE 2015. A CORRECTION OF FIELDS # D1 BRAND NAME, D2 # PRODUCT CODE AND # COMMON DEVICE NAME, # D4 VERSION OR MODEL # AND CATALOG # WERE REQUIRED. D1 - BRAND NAME - PREVIOUS BRAND NAME: SUPPORT ARM 176, CORRECTED BRAND NAME: SERVO-I BASE UNIT D2A - COMMON DEVICE NAME - PREVIOUS COMMON DEVICE NAME: SUPPORT, ARM, CORRECTED COMMON DEVICE NAME: VENTILATOR, CONTINUOUS, FACILITY USE. D2B - PRODUCT CODE - PREVIOUS PRODUCT CODE: IOY, CORRECTED PRODUCT CODE: CBK. D4 - VERSION OR MODEL # - PREVIOUS VERSION OR MODEL #: SUPPORT ARM 176, CORRECTED VERSION OR MODEL #: 6487800. D4 - CATALOG # - PREVIOUS CATALOG #: 6405976, CORRECTED CATALOG #: BLANK.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE VENTILATOR'S SUPPORT ARM WAS BROKEN. THERE WAS NO PATIENT HARM REPORTED. MANUFACTURER'S REF. #: (B)(4).

Description of Event or Problem · 0

MANUFACTURER'S REF. #:(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
779635 SERVO-I BASE UNIT VENTILATOR, CONTINUOUS, FACILITY USE CBK MAQUET CRITICAL CARE AB 6487800

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown