FDA Adverse Event Injury Summary report: N

ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT

MDR report key: 3023478 · Received March 27, 2013

Report

Report Number
3005099803-2013-01519
Event Type
Injury
Date Received
March 27, 2013
Date of Event
February 18, 2013
Report Date
March 1, 2013
Manufacturer
BOSTON SCIENTIFIC - SPENCER
Product Code
KNT
PMA / PMN Number
K031538
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SE
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE COMPLAINANT WAS UNABLE TO PROVIDE THE SUSPECT DEVICE LOT NUMBER; THEREFORE, THE LOT EXPIRATION AND DEVICE MANUFACTURE DATES ARE UNKNOWN. (B)(4) FOR THE REPORTED EVENT OF PEG TUBE DEFORMATION. THE COMPLAINANT INDICATED THAT THE DEVICE WILL NOT BE RETURNED FOR EVALUATION; THEREFORE A FAILURE ANALYSIS OF THE COMPLAINT DEVICE COULD NOT BE COMPLETED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED, A SUPPLEMENTAL MEDWATCH WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT AN ENDOVIVE INITIAL PLACEMENT PEG KIT WAS USED DURING A PROCEDURE (DATE IS UNKNOWN). ACCORDING TO THE COMPLAINT, THERE WAS DEFORMATION OF THE PEG TUBE. THE DEVICE HAD BEEN IN PLACE APPROXIMATELY TWO AND A HALF YEARS AND WAS REPLACED. THE EXACT DATE IS UNKNOWN HOWEVER REPORTED TO BE THE END OF (B)(6) 2013. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION REGARDING THE CIRCUMSTANCES SURROUNDING THIS EVENT HAVE BEEN UNSUCCESSFUL TO DATE. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
126356 ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT TUBES, GASTROINTESTINAL (AND ACCESSORIES) KNT BOSTON SCIENTIFIC - SPENCER UNK518

Patients

Seq Age Sex Outcome Treatment
1 77 YR Other DUODOPA