FDA Adverse Event Injury Summary report: N

QUATTRODE, 30-CM LENGTH PERCUTANEOUS LEAD

MDR report key: 2143077 · Received June 23, 2011

Report

Report Number
1627487-2011-03147
Event Type
Injury
Date Received
June 23, 2011
Date of Event
May 25, 2011
Report Date
May 25, 2011
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
GZB
PMA / PMN Number
K072462
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

MANUFACTURER'S EVAL: THE RETURNED PRODUCT WAS NOT ANALYZED AS THE PRODUCT WAS NOT ANALYZED AS THE COMPLAINT OF INFECTION COULD NOT BE CONFIRMED VIA LABORATORY TESTING. METHOD: THE DEVICE HISTORY AND STERILIZATION RECORDS WERE REVIEWED. RESULTS: THE DEVICE HISTORY AND STERILIZATION RECORDS REVIEWED WERE FOUND TO MEET SPECIFICATIONS AND NO ANOMALIES WERE FOUND. CONCLUSION: THE CAUSE OF THE REPORTED COMPLAINT COULD NOT BE DETERMINED FROM THE REVIEW OF THE DHR AND STERILIZATION RECORDS. SJM HAS LIMITED INFO 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. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

DEVICE 3 OF 6. REFERENCE MFR REPORT 1627487-2011-03145, 03146, 03117, 03119, 03123. THE PT REC'D A SCS SYS INCLUDING AN IPG, THREE PERCUTANEOUS LEADS ( FROM 2 SEPARATE LOTS), AN EXTENSION AND LEAD ANCHOR, ON (B)(6) 2011. IT WAS REPORTED THAT THE DEVICE WERE EXPLANTED ON (B)(6) 2011 DUE TO A (B)(6) INFECTION. THE PT WAS TREATED WITH ORAL ANTIBIOTICS AND WOUND CARE. F/U ON THE PT FOUND THAT THE INFECTION HAS RESOLVED, BUT THE PT IS CONTINUING WITH A WOUND CARE REGIMEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUATTRODE, 30-CM LENGTH PERCUTANEOUS LEAD SPINAL CORD STIMULATION LEAD GZB ST. JUDE MEDICAL - NEUROMODULATION 3163 3269298

Patients

Seq Age Sex Outcome Treatment
1 75 YR Required Intervention