FDA Adverse Event Malfunction Summary report: N

8CH INFINITY DBS LEAD KIT, 40CM, 0.5, B

MDR report key: 8060869 · Received November 12, 2018

Report

Report Number
1627487-2018-11925
Event Type
Malfunction
Date Received
November 12, 2018
Date of Event
October 7, 2018
Report Date
November 28, 2018
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
MHY
UDI-DI
05415067020680
PMA / PMN Number
P140009
Removal / Correction Number
1627487-10/16/18-001-R
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

A CORRECTIVE/PREVENTIVE ACTION PLAN HAS BEEN INITIATED BY THE MANUFACTURER TO ADDRESS THIS ISSUE. THE MANUFACTURER HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. THE MANUFACTURER DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION WAS OBTAINED.

Description of Event or Problem · 1

THE RECORD IS BEING PROACTIVELY INITIATED BASED ON THE ACKNOWLEDGED IMPLANTED OR UNKNOWN STATUS WHICH WAS IN RESPONSE TO THE MEDICAL DEVICE RECALL REMOVAL ACTIVITY, LETTER DATED 11OCT2018. THE LISTED SERIAL NUMBER FOR THE INFINITY DBS (DEEP BRAIN STIMULATION) LEAD MAY CONTAIN AN ELECTRODE THAT WAS NOT MANUFACTURED ACCORDING TO SPECIFICATION. NO CONSEQUENCES OR IMPACT TO THE PATIENT HAVE BEEN REPORTED.

Description of Event or Problem · 1

ADDITIONAL INFORMATION RECEIVED INDICATED THE RADIOGRAPH IS NORMAL; THEREFORE, THE MATERIAL SEGREGATION ISSUE DESCRIBED IN FSCA 1627487-10/16/18-001-R DID NOT AFFECT THIS LEAD. NO ADDITIONAL ACTION WITH THE PATIENT IS NECESSARY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
900806 8CH INFINITY DBS LEAD KIT, 40CM, 0.5, B DBS LEAD MHY ST. JUDE MEDICAL - NEUROMODULATION 6172 6371718 05415067020680

Patients

Seq Age Sex Outcome Treatment
1