FDA Adverse Event Malfunction Summary report: N

MEMBRANE SET COMPLETE

MDR report key: 4374535 · Received December 23, 2014

Report

Report Number
8010762-2014-01374
Event Type
Malfunction
Date Received
December 23, 2014
Date of Event
November 13, 2014
Report Date
December 2, 2014
Manufacturer
MAQUET CARDIOPULMONARY AG
Product Code
DTZ
PMA / PMN Number
K101153
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
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 WAS 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 QUALITY CONTROL PROCESS CONFIRMS THAT 100% FUNCTIONAL INSPECTION FOR LEAKAGE IS PERFORMED DURING PRODUCTION. MAQUET CARDIOPULMONARY (B)(4) HAS INITIATED AN INTERNAL PROCESS ((B)(4)) TO ADDRESS THE APPROPRIATE CORRECTIVE AND PREVENTIVE ACTION. A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED WHEN NEW INFORMATION BECOMES AVAILABLE. ADDITIONAL INFORMATION: THE PRODUCT MENTIONED UNDER SECTION D IS NOT DISTRIBUTED TO THE US, BUT THE PRODUCT WITH CONTRIBUTING DESIGN FUNCTION TO THE AFFECTED COMPONENT (QUADROX-ID) IS REGISTERED UNDER 510 (K): K101153.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING USE, BLOOD LEAKAGE AS DROPS WERE NOTED AT THE DEVICE GAS OUTLET. BLOOD LOSS WAS 2-3 ML. THE DEVICE WAS NOT REPLACED. NO REPORTED PATIENT EFFECT. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
847281 MEMBRANE SET COMPLETE HQC 7001 #MEMBRANE SET COMPLETE DTZ MAQUET CARDIOPULMONARY AG HQV 7001 92141483

Patients

Seq Age Sex Outcome Treatment
1