FDA Adverse Event Injury Summary report: N

MULTI-LINK 8

MDR report key: 2193532 · Received August 5, 2011

Report

Report Number
2024168-2011-05563
Event Type
Injury
Date Received
August 5, 2011
Date of Event
July 9, 2011
Report Date
July 12, 2011
Manufacturer
AV-TEMECULA-CT
Product Code
MAF
PMA / PMN Number
P020047
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). DURING PROCESSING OF THIS COMPLAINT, ATTEMPTS WERE MADE TO OBTAIN COMPLETE EVENT, PATIENT AND DEVICE INFORMATION. THERE WAS NO REPORTED PRODUCT DEFICIENCY. THE REPORTED PATIENT EFFECTS OF ANGINA AND RESTENOSIS, AS LISTED IN THE MULTI-LINK 8 INSTRUCTIONS FOR USE, ARE KNOWN ADVERSE EVENTS ASSOCIATED WITH CORONARY STENTING PROCEDURES. ALTHOUGH A CONCLUSIVE CAUSE FOR THE REPORTED PATIENT EFFECTS AND THE RELATIONSHIP TO THE DEVICE, IF ANY, COULD NOT BE DETERMINED, THERE IS NO INDICATION OF A PRODUCT QUALITY DEFICIENCY WITH RESPECT TO MANUFACTURE, DESIGN OR LABELING.

Description of Event or Problem · 1

IT WAS REPORTED THAT ON (B)(6) 2011 DURING THE PROCEDURE IN THE LEFT ANTERIOR DESCENDING ARTERY, A 3.5 X 15 MULTILINK 8 WAS SUCCESSFULLY IMPLANTED. THE PATIENT WAS REPORTED AS FINE AND STABLE. ON (B)(6) 2011, THE PATIENT COMPLAINED OF CHEST PAIN. REPEAT ANGIOGRAPHY REVEALED INSTENT RESTENOSIS. BALLOON ANGIOPLASTY WAS PERFORMED; HOWEVER, THE PHYSICIAN STATED AN ADDITIONAL STENT WILL NEED TO BE IMPLANTED FOR TREATMENT OF THE RESTENOSIS. REPORTEDLY, THE PATIENT CANNOT FINANCIALLY AFFORD A DRUG ELUTING STENT; THEREFORE, RE-INTERVENTION IS STILL UNDETERMINED. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MULTI-LINK 8 CORONARY STENT SYSTEM MAF AV-TEMECULA-CT 0012961

Patients

Seq Age Sex Outcome Treatment
1 70 YR Hospitalization| R