FDA Adverse Event Death Summary report: N

HORIZON APPLIER MEDIUM APPLIER 11" CURVED

MDR report key: 2133308 · Received June 15, 2011

Report

Report Number
1044475-2011-00062
Event Type
Death
Date Received
June 15, 2011
Date of Event
May 13, 2011
Report Date
May 23, 2011
Manufacturer
TELEFLEX MEDICAL
Product Code
FZP
PMA / PMN Number
EXEMPT
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
RISK MANAGER

Narratives

Additional Manufacturer Narrative · 1

THERE IS NO DEVICE SAMPLE AVAILABLE FOR INVESTIGATION. INVESTIGATION IS INCOMPLETE AT TIME OF THIS REPORT. A FOLLOW-UP INVESTIGATION REPORT WILL BE SENT WHEN COMPLETED.

Description of Event or Problem · 1

INFORMATION OBTAINED FROM MEDWATCH. COMPLAINT ALLEGES: PATIENT HAD A KIDNEY TRANSPLANT ON (B)(6) 2011, WHICH FAILED. ON (B)(6) 2011, PATIENT HAD THE REJECTED KIDNEY REMOVED. PATIENT THEN EXHIBITED SYMPTOMS OF HYPOVOLEMIA SEVEN HOURS POST-OP AND RETURNED TO THE OPERATING ROOM. TITANIUM LIGATING CLIPS WERE USED ON THE RENAL ARTERY DURING THE ALLOGRAFT NEPHRECTOMY SURGERY. PATIENT WAS REOPENED POST-OPERATIVELY AND THE RENAL ARTERY WAS OPEN AND ACTIVELY BLEEDING. THE PATIENT EXPIRED IN THE OPERATING ROOM. TWO APPLIERS HAD BEEN USED: ONE LARGE AND ONE MEDIUM. TWO SIZES OF CLIPS WERE USED: MEDIUM AND LARGE. IT IS UNCLEAR WHICH SIZE CLIP WAS USED AT THE LOCATION WHERE THE BLEEDING OCCURRED. THERE ARE NO SAMPLES AVAILABLE FOR INVESTIGATION. NO AUTOPSY WAS PERFORMED PER THE RISK MANAGER. REFERENCE MDR# FOR OTHER CLIPS AND APPLIER: MDR# 3003898360-2011-00277, MDR# 3003898360-2011-00278, MDR# 1044475-2011-00066.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HORIZON APPLIER MEDIUM APPLIER 11" CURVED LIGATING CLIP APPLIER FZP TELEFLEX MEDICAL NA 04L0700032

Patients

Seq Age Sex Outcome Treatment
1 43 YR Death HORIZON TITANIUM LARGE CLIP, (B)(4)| HORIZON TITANIUM MEDIUM CLIP, (B)(4)| HORIZON LARGE APPLIER 11" CURVED, (B)(4)