FDA Adverse Event Injury Summary report: N

HAKIM VENTRICULAR & PERITONEAL CATHETERS WITH BACTISEAL

MDR report key: 4808573 · Received June 1, 2015

Report

Report Number
1226348-2015-10303
Event Type
Injury
Date Received
June 1, 2015
Date of Event
May 5, 2015
Manufacturer
CODMAN & SHURTLEFF, INC. / MEDOS S.A.
Product Code
JXG
PMA / PMN Number
PK003322
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). UPON COMPLETION OF THE INVESTIGATION, A FOLLOW UP REPORT WILL BE FILED.

Additional Manufacturer Narrative · 1

(B)(4).IT WAS NOT POSSIBLE TO INVESTIGATE THE PRODUCTS SINCE THEY WERE NOT RETURNED FOR EVALUATION. IF THE DEVICES ARE RETURNED IN THE FUTURE, THIS COMPLAINT WILL BE RE-OPENED AND EVALUATED. REVIEW OF THE HISTORY DEVICE RECORDS CONFIRMED THE VALVE PRODUCT CODE 82-3114 WITH LOT CRCC05, CONFORMED TO THE SPECIFICATIONS WHEN RELEASED TO STOCK ON THE APRIL 24TH, 2014. REVIEW OF THE HISTORY DEVICE RECORDS CONFIRMED THE CATHETER PRODUCT CODE 82-3072 WITH LOT CRJB8K, CONFORMED TO THE SPECIFICATIONS WHEN RELEASED TO STOCK ON THE AUGUST 20TH, 2014. BASED ON THE RESULTS OF THIS INVESTIGATION NO FURTHER ACTION IS REQUIRED. TRENDS WILL BE MONITORED FOR THIS AND SIMILAR COMPLAINTS. AT THE PRESENT TIME THIS COMPLAINT IS CLOSED.

Description of Event or Problem · 1

THE PATIENT IS MALE AND (B)(6) YEARS OLD, DID V-P SURGERY ON 11ST (B)(6) 2015. THE PATIENT NOTED LEAKAGE OF LIQUID FROM BELLY. IT WAS REPORTED THAT PATIENT HAD SUBCUTANEOUS INFECTION. THE SURGEON INTENDED TO DO THE TREATMENT OF INFLAMMATION AND REMOVE THE PROGRAMMER. THE PATIENT IS STABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352709 HAKIM VENTRICULAR & PERITONEAL CATHETERS WITH BACTISEAL SHUNT, CENTRAL NERVOUS SYS & COMPS JXG CODMAN & SHURTLEFF, INC. / MEDOS S.A. CRJB8K

Patients

Seq Age Sex Outcome Treatment
1 34 YR Required Intervention 823114