FDA Adverse Event Injury Summary report: N

PRECISE OTW NITINOL STENT

MDR report key: 1171201 · Received September 22, 2008

Report

Report Number
9616099-2008-02294
Event Type
Injury
Date Received
September 22, 2008
Date of Event
August 25, 2008
Report Date
August 26, 2008
Manufacturer
CORDIS DE MEXICO
Product Code
NIM
PMA / PMN Number
P030047
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE PRODUCT IS NOT AVAILABLE FOR EVAL. THIS IS ONE OF TWO PRODUCTS INVOLVED IN THE SAME PATIENT AND REPORTED UNDER MANUFACTURING NUMBERS: 1016427-2008-00246 AND 961609-2008-02294. ADD'L INFO WILL BE SUBMITTED WITHIN 30 DAYS UPON RECEIPT.

Description of Event or Problem · 1

THE REPORT RECEIVED INDICATED THAT DURING A CAROTID ARTERY STENTING PROCEDURE, THE 6MM ANGIOGUARD WAS DELIVERED WITHOUT DIFFICULTIES. THE TARGET LESION WAS PRE-DILATED TO 10 ATMOSPHERES (ATMS) AND WAS SUBSEQUENTLY STENTED WITH A 10X40MM PRECISE STENT, THE LESION WAS POST-DILATED TO 8 ATMS. AFTER POST-DILATION, THE BLOOD FLOW STOPPED. THEREFORE, THE PHYSICIAN SUCTIONED THE BLOOD THREE TIMES AND THEN THE BLOOD FLOW WAS RECOVERED. THE ANGIOGUARD WAS RETRIEVED WITH THE CAPTURE SHEATH AND THE PROCEDURE WAS COMPLETED WITHOUT OTHER PROBLEMS. HOWEVER, THE PT EXPERIENCED MILD PARALYSIS ON HIS LEFT AND CEREBRAL INFARCTION WAS CONFIRMED BY MRI. THE PT IS UNDER TREATMENT CONSERVATIVELY. THE TARGET LESION WAS THE INTERNAL CAROTID ARTERY PRESENTING MILD CALCIFICATION AND TORTUOUSITY WITH A 90% RATE OF STENOSIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRECISE OTW NITINOL STENT SELF EXPANDING STENTS (NIM) NIM CORDIS DE MEXICO NA UNK

Patients

Seq Age Sex Outcome Treatment
1 82 YR Hospitalization BALLOON CATHETER AMIIA (4MM X 40MM)| SUCTION DEVICE (ELIMINATE/CLINICAL SUPPLY)| SHUTTLE SHEATH (COOK)| BOSTON SCIENTIFIC STERING (4.5MM X 30MM)