FDA Adverse Event Injury Summary report: N

PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

MDR report key: 3003833 · Received March 14, 2013

Report

Report Number
2134265-2013-01454
Event Type
Injury
Date Received
March 14, 2013
Report Date
February 13, 2013
Manufacturer
BOSTON SCIENTIFIC - MAPLE GROVE
Product Code
NIQ
PMA / PMN Number
P110010
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

DEVICE IS COMBINATION PRODUCT. DEVICE EVALUATED BY MANUFACTURER: THE DEVICE WAS NOT RECEIVED FOR ANALYSIS. THE BATCH NUMBER IS UNKNOWN AND THE MANUFACTURING RECORDS FOR THE COMPLAINT DEVICE COULD NOT BE REVIEWED. THE ROOT CAUSE IS ANTICIPATED PROCEDURAL COMPLICATIONS AS THIS EVENT IS A KNOWN PHYSIOLOGICAL EFFECT OF THE PROCEDURE AND IS NOTED WITHIN THE DFU. (B)(4).

Description of Event or Problem · 1

SAME CASE AS MDR ID# 2134265-2013-01453. SAME CASE AS MDR ID# 2134265-2013-01455. (B)(4). IT WAS REPORTED POST A PERCUTANEOUS CORONARY INTERVENTION PROCEDURE, THE PATIENT EXPERIENCED AN ALLERGIC REACTION. IN (B)(6) 2012, THE 99% STENOSED AND 10MM LONG DE-NOVO TARGET LESION WAS LOCATED IN MID LEFT ANTERIOR DESCENDING ARTERY WITH A REFERENCE VESSEL DIAMETER OF 3.0MM. THE TARGET LESION WAS TREATED WITH PRE-DILATION AND PLACEMENT OF A TWO 3.0X12MM AND A 3.50X12MM PROMUS ELEMENT PLUS STENT, RESULTING IN 0% RESIDUAL STENOSIS FOLLOWING POST DILATION. THE FOLLOWING DAY THE PATIENT WAS DISCHARGED ON CLOPIDOGREL AND ASPIRIN. IN (B)(6) 2013, THAT PATIENT EXPERIENCED AN ALLERGIC REACTION AND WAS HOSPITALIZED. THE PATIENT WAS TREATED WITH MEDICATIONS AND THE EVENT WAS CONSIDERED RECOVERING/RESOLVING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
107322 PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM STENT, CORONARY, DRUG-ELUTING NIQ BOSTON SCIENTIFIC - MAPLE GROVE UNK717

Patients

Seq Age Sex Outcome Treatment
1 76 YR Required Intervention