FDA Adverse Event Malfunction Summary report: N

ELECTA WASH SET 225 ML BOWL

MDR report key: 779072 · Received August 30, 2006

Report

Report Number
1718850-2006-00029
Event Type
Malfunction
Date Received
August 30, 2006
Date of Event
July 18, 2006
Report Date
July 18, 2006
Manufacturer
SORIN GRP ITALIA S.R.I., A SORIN GRP CO, DISTRIBUTED BY COBE CARDIOVASCULAR, INC
Product Code
CAC
PMA / PMN Number
K020647
Removal / Correction Number
PENDING
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

H6 THE CONCLUSION IS BASED ON EVALUATION OF WASH SETS IN A BRACKET THAT INCLUDED THIS LOT. THE EVALUATION REVEALED THAT IF THE BOWL CANNOT BE INSERTED IN ACCORDANCE WITH THE INSTRUCTIONS FOR USE, THERE IS A RISK THAT THE BOWL'S ROTATING SEAL AREA COULD DETERIORATE DURING CENTRIFUGING, RELEASING PARTICULATE INTO THE PROCESSED BLOOD. THE LOADING OF WASH SETS FROM THIS BRACKET OF PRODUCT CAN BE MORE DIFFICULT DUE TO A MANUFACTURING PROCESS ERROR THAT RESULTED IN A SLIGHT DEFORMATION IN THE MOUNTING RING ON THE BOWL BOTTOM. THE PROCESS ERROR HAS SUBSEQUENTLY BEEN CORRECTED BY THE MANUFACTURER. BASED ON THE EVENT DESCRIBED IN G4 ABOVE, SORIN GROUP ITALIA COMPLETED A RISK ASSESSMENT THAT LEAD TO A FIELD NOTIFICATION. THE FIELD NOTIFICATION IN THE U.S. WAS CONDUCTED BY COBE CARDIOVASCULAR, INC., THE DISTRIBUTOR OF THIS DEVICE. THE Z-NUMBER WILL BE PROVIDED WHEN IT IS AVAILABLE FROM THE LOCAL FDA OFFICE.

Description of Event or Problem · 1

THE CUSTOMER EXPERIENCED NOISE COMING FROM 2 WASH SETS OF THIS LOT. IN ONE INCIDENT, THE WASH SET WAS SO NOISY, THE MACHINE AND WASH SET WERE REMOVED FROM THE ROOM. THAT WASH SET WAS DISCARDED. IN THE SECOND INCIDENT, THE BOWL WAS ALSO NOISY. IT WAS USED THROUGHOUT THE CASE AND RETURNED TO THE DISTRIBUTOR FOR EVALUATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ELECTA WASH SET 225 ML BOWL APPARATUS, AUTOTRANSFUSION CAC SORIN GRP ITALIA S.R.I., A SORIN GRP CO, DISTRIBUTED BY COBE CARDIOVASCULAR, INC NA 0603030049

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN