NC EUPHORA RX
Report
- Report Number
- 9612164-2018-03554
- Event Type
- Injury
- Date Received
- December 11, 2018
- Date of Event
- December 13, 2017
- Report Date
- March 14, 2019
- Manufacturer
- MEDTRONIC MEXICO,
- Product Code
- LOX
- PMA / PMN Number
- K141090
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- PHYSICIAN
Narratives
IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
CEC ADJUDICATION; CEC ADJUDICATED STENT THROMBOSIS AS NOT AN EVENT. CEC ADJUDICATED NON Q WAVE MI (TV) AS A NON EVENT. PATIENT HAS A MEDICAL HISTORY OF HYPERLIPIDEMIA, CHRONIC RENAL INSUFFICIENCY, MULTI-VESSEL CORONARY ARTERY DISEASE, AND PREVIOUS PCI. DURING THE INDEX PROCEDURE, TWO RESOLUTE ONYX DRUG-ELUTING STENTS WERE IMPLANTED IN THE 1ST DIAGONAL AND THREE IMPLANTED IN THE LAD. ORBITAL ATHERECTOMY OF LAD WAS ALSO PERFORMED. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
CEC ADJUDICATION STILL NON-Q-WAVE MI (TARGET VESSEL), MDT EXTENDED HISTORICAL PERI-PCI. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
DURING INDEX PROCEDURE FIVE RESOLUTE ONYX DRUG ELUTING STENTS WERE IMPLANTED; FOUR IN THE LAD AND ONE IN THE 1ST DIAGONAL AND TWO NC EUPHORA BALLOONS WERE USED IN THE LAD. ON THE SAME DAY THE PATIENT SUFFERED ELEVATED TROPONIN AND RECOVERED THE FOLLOWING DAY. CEC ADJUDICATED THE EVENT AS NON-Q WAVE MYOCARDIAL INFARCTION OF THE TARGET VESSEL. INVESTIGATOR ASSESSED THE EVENT IS UNLIKELY RELATED TO DEVICE AND NOT RELATED TO ANTIPLATELET MEDICATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 991109 | NC EUPHORA RX | CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS | LOX | MEDTRONIC MEXICO, |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 80 YR | Hospitalization |