FDA Adverse Event Malfunction Summary report: N

SPS-1

MDR report key: 6285504 · Received January 30, 2017

Report

Report Number
6285504
Event Type
Malfunction
Date Received
January 30, 2017
Date of Event
November 19, 2016
Report Date
January 27, 2017
Manufacturer
ORGAN RECOVERY SYSTEMS, INC.
Product Code
KDL
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

TRANSPLANT ADMINISTRATION RECEIVED AN EMAIL FROM OUR ORGAN PROCUREMENT AGENCY THAT OUR RECIPIENT RECEIVED A LIVER GRAFT THAT WAS PERFUSED WITH A RECALLED BATCH OF ORGAN PRESERVATION SOLUTION. WE WERE MADE AWARE OF A VOLUNTARY RECALL ON CERTAIN BATCHES OF ORGAN PRESERVATION SOLUTION CALLED STATIC PRESERVATION SOLUTION -1 (SPS-1), MANUFACTURED BY ORGAN RECOVERY SYSTEMS. THE RECALL WAS DUE TO A REPORT BY ANOTHER OPO REGARDING BACTERIAL CONTAMINATION. ACCORDING TO THE REPORT THE SOLUTION SAMPLES OBTAINED FROM SEVERAL OPENED BAGS WERE POSITIVE FOR PANTOEA AGGLOMERANS AND ENTEROCOCCUS CASSELIFLAVUS. THIS MICROBIAL GROWTH WAS REPORTED FOR TWO LOTS OF THE PRESERVATION SOLUTION SPS-1.LOTS: PBR-0074-330 AND PBR-0060-392, EXPIRATION 06/01/2018. OUR PHARMACY WAS MADE AWARE OF THE RECALL SHORTLY AFTER WE RECEIVED NOTICE FROM THE FIRST OPO OVER THE WEEKEND. PHARMACY AND THE OPERATING ROOM IMMEDIATELY QUARANTINED ANY UNUSED INVENTORY FROM THE AFFECTED LOTS. THE PATIENT IS AT HOME AND IS AFEBRILE. AT THE RECOMMENDATION OF OUR ID TEAM WE WILL BE OBTAINING ONE SET OF BLOOD CULTURES ON THIS RECIPIENT AT THEIR NEXT BLOOD DRAW.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
70084 SPS-1 ORGAN PRESERVATION SOLUTION KDL ORGAN RECOVERY SYSTEMS, INC. PBR-0074-330

Patients

Seq Age Sex Outcome Treatment
1 65 YR