HORIZON APPLIER MEDIUM APPLIER 11" CURVED
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
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.
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) |