FDA Adverse Event Death Summary report: N

SYNCARDIA FREEDOM DRIVER

MDR report key: 6068439 · Received October 31, 2016

Report

Report Number
3003761017-2016-00344
Event Type
Death
Date Received
October 31, 2016
Date of Event
October 2, 2016
Report Date
October 2, 2016
Manufacturer
SYNCARDIA SYSTEMS, LLC
Product Code
LOZ
UDI-DI
00858000003121
PMA / PMN Number
P030011
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE FREEDOM DRIVER HAS BEEN RETURNED TO SYNCARDIA FOR EVALUATION. THE RESULTS OF THE INVESTIGATION WILL BE PROVIDED IN A FOLLOW-UP MDR. (B)(4).

Additional Manufacturer Narrative · 1

THE FREEDOM DRIVER WAS RETURNED TO SYNCARDIA FOR EVALUATION. VISUAL INSPECTION OF THE DRIVER'S INTERIOR REVEALED EVIDENCE OF LIQUID INGRESS INTO THE CASE, DARK RESIDUE AROUND THE PRIMARY MOTOR GEARBOX EXTERNAL SURFACES, AND A SECONDARY MOTOR CONTROLLER CABLE THAT WAS NOT CONNECTED. THE LIQUID INGRESS WAS EVIDENCED BY PUDDLE-LIKE VERDIGRIS ON THE CASE INTERIOR ORIGINATING AT THE DRIVELINE ENTRY PORT. THE PRIMARY MOTOR GEARBOX WAS FOUND TO DISPLAY DARK RESIDUE AND RESISTANCE TO SPINNING WAS MUCH GREATER WHEN COMPARED TO THE SECONDARY MOTOR. THERE WAS EVIDENCE OF CORROSION. DURING DISASSEMBLY, THE PRIMARY MOTOR GEARBOX WAS FOUND TO BE HEAVILY DEGRADED, AND ANY REMAINING LUBRICANT IN THE BEARINGS WAS FOUND TO BE SEVERELY OVERHEATED. ANALYSIS OF THE VERDIGRIS SUGGESTS THAT THE LIQUID THAT CAME INTO THE DRIVER MAY HAVE BEEN A CHLORINATED CLEANING (SURFACTANT) SOLUTION. THE ELECTRONIC DATA (EEPROM) SHOWED AGREEMENT WITH THE CUSTOMER-REPORTED ISSUE AND INDICATED THAT THE DRIVER CEASED PUMPING. AS RECEIVED, THE SECONDARY MOTOR CONTROLLER CABLE WAS INTACT BUT NOT CONNECTED TO THE MAIN PRINTED CIRCUIT BOARD ASSEMBLY (PCBA). IT COULD NOT BE CONCLUSIVELY DETERMINED WHY THE SECONDARY MOTOR CONTROLLER CABLE WAS NOT CONNECTED TO THE MAIN PCBA IN THE DRIVER, BUT THE MOST LIKELY ROOT CAUSE IS AN INCOMPLETE CONNECTION DURING SERVICING. INVESTIGATION TESTING CONDUCTED ON THE DRIVER RESULTED IN THE OBSERVATION THAT THE PRIMARY MOTOR WOULD OVERHEAT AND EVENTUALLY ALARM, CULMINATING IN A SWITCH OVER TO SECONDARY MOTOR OPERATION. ALTHOUGH IT COULD NOT BE DEFINITIVELY PROVEN THAT THE OBSERVED EVIDENCE OF LIQUID INGRESS CAUSED THE PRIMARY MOTOR TO STOP, A MOTOR GEARBOX EXPOSED TO CHLORINATED SURFACTANTS IS LIKELY TO EXPERIENCE ACCELERATED WEAR SIMILAR TO WHAT WAS OBSERVED WITHIN THE EVENT PRIMARY MOTOR GEARBOX. FREEDOM DRIVER S/N (B)(4) STOPPED BECAUSE OF THE CESSATION OF THE PRIMARY MOTOR GEARBOX CAUSED BY EXCESSIVE HEAT GENERATION, COUPLED WITH A SECONDARY MOTOR CONTROLLER CABLE THAT WAS NOT CONNECTED TO THE MAIN PCBA OF THE DRIVER. FREEDOM DRIVER SYSTEM GUIDEBOOK FOR PATIENTS AND CAREGIVERS, CONTAINS LANGUAGE (SECTION 9.1.1) REGARDING DRIVER CLEANING AND MAINTENANCE, WHICH INSTRUCTS THE USER HOW THE DRIVER IS TO BE HANDLED AROUND LIQUIDS AND CLEANING MATERIALS: DO NOT SUBMERGE THE FREEDOM DRIVER OR EXPOSE IT TO WATER; DO NOT USE PAINT REMOVER, FINGERNAIL POLISH REMOVER, OR OTHER SOLVENTS ANYWHERE NEAR THE FREEDOM DRIVER; USE EXTREME CARE WHEN CLEANING THE EQUIPMENT. DUST THE EQUIPMENT PERIODICALLY WITH A SOFT, CLEAN CLOTH; IF YOU NEED TO REMOVE HEAVY DIRT FROM THE OUTSIDE OF THE FREEDOM DRIVER, USE A SOFT, CLEAN LIGHTLY DAMPENED CLOTH; DAMPEN THE CLOTH WITH MILD SOAP AND WATER SOLUTION AND WIPE GENTLY; DO NOT SOAK ANY ITEM OF THE FREEDOM DRIVER DURING CLEANING; DO NOT ALLOW WATER TO COME IN DIRECT CONTACT WITH THE FREEDOM DRIVER ELECTRICAL CONNECTIONS. THIS ISSUE WILL CONTINUE TO BE MONITORED AND TRENDED AS PART OF THE CUSTOMER EXPERIENCE PROCESS. SYNCARDIA HAS COMPLETED ITS EVALUATION OF THIS COMPLAINT AND IS CLOSING THIS FILE. (B)(4).

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE PATIENT'S WIFE HEARD HIS FREEDOM DRIVER ALARM AND FOUND THE PATIENT UNRESPONSIVE. THE CUSTOMER ALSO REPORTED THAT THE WIFE CALLED THE CEDARS-SINAI MEDICAL CENTER AND WAS CONNECTED TO A VAD COORDINATOR, WHO WAS ABLE TO HEAR AN AUDIBLE FAULT ALARM FROM THE FREEDOM DRIVER IN THE BACKGROUND. THE CUSTOMER ALSO REPORTED THAT THE VAD COORDINATOR INSTRUCTED THE WIFE TO CHECK THE FREEDOM DRIVER TO SEE IF IT WAS PUMPING. THE WIFE STATED THAT THE FREEDOM DRIVER WAS NOT PUMPING AND THAT THE DISPLAY SCREEN WAS BLANK. THE VAD COORDINATOR ALSO STATED THAT SHE WAS ABLE TO HEAR OVER THE PHONE THAT THE DRIVER WAS NOT PUMPING. THE CUSTOMER ALSO REPORTED THAT THE VAD COORDINATOR TALKED THE WIFE THROUGH SWITCHING THE PATIENT TO HIS BACK-UP FREEDOM DRIVER. AFTER THE SWITCH, THE NEW FREEDOM DRIVER EXHIBITED NO ALARMS. THE CUSTOMER ALSO REPORTED THAT THE PATIENT REMAINED UNRESPONSIVE AND 911 WAS CALLED. THE PATIENT WAS TRANSPORTED TO THE NEAREST ER, WHICH WAS A (B)(6) HOSPITAL AND WAS SUBSEQUENTLY TRANSFERRED TO (B)(6) MEDICAL CENTER. THE CUSTOMER ALSO REPORTED THAT THE PATIENT EXPIRED.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE PATIENT'S WIFE HEARD HIS FREEDOM DRIVER ALARM AND FOUND THE PATIENT UNRESPONSIVE. THE CUSTOMER ALSO REPORTED THAT THE WIFE CALLED THE CEDARS-SINAI MEDICAL CENTER AND WAS CONNECTED TO A VAD COORDINATOR, WHO WAS ABLE TO HEAR AN AUDIBLE FAULT ALARM FROM THE FREEDOM DRIVER IN THE BACKGROUND. THE CUSTOMER ALSO REPORTED THAT THE VAD COORDINATOR INSTRUCTED THE WIFE TO CHECK THE FREEDOM DRIVER TO SEE IF IT WAS PUMPING. THE WIFE STATED THAT THE FREEDOM DRIVER WAS NOT PUMPING AND THAT THE DISPLAY SCREEN WAS BLANK. THE VAD COORDINATOR ALSO STATED THAT SHE WAS ABLE TO HEAR OVER THE PHONE THAT THE DRIVER WAS NOT PUMPING. THE CUSTOMER ALSO REPORTED THAT THE VAD COORDINATOR TALKED THE WIFE THROUGH SWITCHING THE PATIENT TO HIS BACK-UP FREEDOM DRIVER. AFTER THE SWITCH, THE NEW FREEDOM DRIVER EXHIBITED NO ALARMS. THE CUSTOMER ALSO REPORTED THAT THE PATIENT REMAINED UNRESPONSIVE AND 911 WAS CALLED. THE PATIENT WAS TRANSPORTED TO THE NEAREST ER, WHICH WAS A NON-CERTIFIED SYNCARDIA TAH-T HOSPITAL AND WAS SUBSEQUENTLY TRANSFERRED TO (B)(6) MEDICAL CENTER. THE CUSTOMER ALSO REPORTED THAT THE PATIENT EXPIRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
717555 SYNCARDIA FREEDOM DRIVER EXTERNAL PNEUMATIC DRIVER LOZ SYNCARDIA SYSTEMS, LLC 00858000003121

Patients

Seq Age Sex Outcome Treatment
1 57 YR Death