FDA Adverse Event Injury Summary report: N

PERMANENT LIFE SUPPORT SET

MDR report key: 4252638 · Received November 5, 2014

Report

Report Number
8010762-2014-01104
Event Type
Injury
Date Received
November 5, 2014
Date of Event
October 7, 2014
Report Date
October 7, 2014
Manufacturer
MAQUET CARDIOPULMONARY AG
Product Code
DTQ
PMA / PMN Number
K102726
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

MAQUET CARDIOPULMONARY IS AWARE OF SIMILAR COMPLAINTS. THE DEVICES DISPLAYED A SIMILAR MALFUNCTION WHICH WERE TESTED AND EVALUATED UNDER AN OPTICAL MICROSCOPE. DELAMINATION OF SOME GAS FIBERS WERE OBSERVED WHICH ALLOWED FOR THE PRIMING SOLUTION OR BLOOD TO FLOW INSIDE THE GAP BETWEEN THE GAS FIBERS AND POLYURETHANE. GRAVITY THEN ALLOWED FOR PASSAGE TO THE GAS EXITING PATH ALONG THE HOUSING. THE MOST PROBABLE ROOT-CAUSE IS THE DELAMINATION OF THE HOLLOW GAS FIBERS FROM THE POLYURETHANE POTTING AREA. A REVIEW OF THE QUAL CONTROL PROCESS CONFIRMS THAT 100% FUNCTIONAL INSPECTION FOR LEAKAGE IS PERFORMED DURING PRODUCTION. MAQUET CARDIOPULMONARY AG HAS INITIATED AN INTERNAL PROCESS (CAPA-(B)(4) TO ADDRESS THE APPROPRIATE CORRECTIVE AND PREVENTATIVE ACTION. A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED IF NEW INFO BECOMES AVAILABLE.

Description of Event or Problem · 1

IT WAS REPORTED THAT APPROXIMATELY TWO HOURS AFTER INITIATION OF VA ECMO SUPPORT, LEAKAGE FROM THE GAS OUTLET WAS OBSERVED. THE DEVICE WAS CHANGED OUT WITH NO SIGNIFICANT BLOOD LOSS REPORTED. (B)(4). ABBREVIATIONS: VA ECMO = VENOUS ARTERIAL EXTRACORPOREAL MEMBRANE OXYGENATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
710127 PERMANENT LIFE SUPPORT SET DTQ MAQUET CARDIOPULMONARY AG BE-PLS 2050 70097044

Patients

Seq Age Sex Outcome Treatment
1