FDA Adverse Event Malfunction Summary report: N

CAMINO ICP MONITORING CATHETER W/ INTEGRATED LIC

MDR report key: 6307471 · Received February 7, 2017

Report

Report Number
2023988-2017-00017
Event Type
Malfunction
Date Received
February 7, 2017
Report Date
January 19, 2017
Manufacturer
INTEGRA NEUROSCIENCES CA/USA
Product Code
GWM
PMA / PMN Number
K102875
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

IT IS UNKNOWN IF THE DEVICE INVOLVED IN THE REPORTED INCIDENT IS EXPECTED TO BE RETURNED FOR EVALUATION. AN INVESTIGATION HAS BEEN INITIATED BASED UPON THE REPORTED INFORMATION.

Additional Manufacturer Narrative · 1

INTEGRA HAS COMPLETED THEIR INTERNAL INVESTIGATION ON MARCH 16, 2017. THE INVESTIGATION INCLUDED: METHODS: REVIEW OF DEVICE HISTORY RECORDS. REVIEW OF COMPLAINTS HISTORY. RESULTS: THE CATHETER HAS NOT BEEN RETURNED FOR INVESTIGATION. DHR REVIEW; THERE WERE 12 LOTS MODEL 110-4L SHIPPED TO THE CUSTOMER FROM JANUARY 1ST 2016 TO JANUARY 15TH 2017; THEIR BATCH HISTORY RECORDS INDICATING THAT ALL REQUIREMENTS MET BEFORE THEY WERE RELEASED TO FINISHED GOODS. COMPLAINTS HISTORY; THERE WERE 12 OTHER COMPLAINTS THAT ISSUED WITH COMPLAINT CODE PERF032, AND ONE OF THEM WAS CONFIRMED. FAILURE RATE PERCENTAGE (B)(4). CONCLUSION: COULD NOT BE CONFIRM SINCE THE CUSTOMER DID NOT RETURN THE DEVICE FOR EVALUATION.

Description of Event or Problem · 1

THE PROBES ARE GIVING ERRATIC READINGS. THE HOSPITAL IS A REGULAR USER WITH GOOD EXPERIENCE. ADDITIONAL INFORMATION HAS BEEN REQUESTED. LINKED TO MFG. REPORT NUMBERS: 2023988-2017-00012, 2023988-2017-00013, 2023988-2017-00014, 2023988-2017-00015, 2023988-2017-00016, 2023988-2017-00011, 2023988-2017-00018.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
91910 CAMINO ICP MONITORING CATHETER W/ INTEGRATED LIC N/A GWM INTEGRA NEUROSCIENCES CA/USA

Patients

Seq Age Sex Outcome Treatment
1 CAMINO MONITOR