PERMANENT LIFE SUPPORT SET
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
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.
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 |