FDA Adverse Event Malfunction Summary report: N

MPS DELIVERY SET W AA AND ADD CASSETTES

MDR report key: 2920176 · Received December 11, 2012

Report

Report Number
1649914-2012-00035
Event Type
Malfunction
Date Received
December 11, 2012
Date of Event
November 12, 2012
Report Date
November 14, 2012
Manufacturer
QUEST MEDICAL, INC.
Product Code
DTR
PMA / PMN Number
K953838
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). QUEST MEDICAL, INC. HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. QUEST MEDICAL, INC. DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

IT WAS REPORTED BY THE HOSPITAL PERFUSIONIST THAT DURING A PROCEDURE THE DELIVERY SET DISPOSABLE EXPERIENCED A BLOOD LEAK WITHIN THE HEAT EXCHANGER. THE PERFUSIONIST CONTINUED TO USE THE DEVICE TO SUCCESSFULLY COMPLETE THE PROCEDURE WITH NO PATIENT COMPLICATIONS REPORTED. THE DISPOSABLE DEVICE WAS RETURNED TO THE MANUFACTURER FOR ANALYSIS. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION FROM THE HOSPITAL WERE UNSUCCESSFUL. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MPS DELIVERY SET W AA AND ADD CASSETTES CPBP HEAT EXCHANGER DTR QUEST MEDICAL, INC. 5001102 0422502E07

Patients

Seq Age Sex Outcome Treatment
1