FDA Adverse Event Injury Summary report: N

CP COVERED STENT

MDR report key: 17525572 · Received August 12, 2023

Report

Report Number
MW5132513
Event Type
Injury
Date Received
August 12, 2023
Report Date
August 8, 2012
Manufacturer
NUMED, INC
Product Code
PNF
Report Source
Voluntary report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

MEDTRONIC RECEIVED INFORMATION THAT FLUOROSCOPY REVEALED THERE WAS A SINGLE STRUT FRACTURE IN THE ANTERIOR PROXIMAL ASPECT OF THE NUMED CP COVERED STENT (UNKNOWN MODEL/SERIAL NUMBER). NO ADDITIONAL DETAILS WERE PROVIDED. N/A. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2219615 CP COVERED STENT AORTIC STENT PNF NUMED, INC

Patients

Seq Age Sex Outcome Treatment
1 Unknown