FDA Adverse Event Injury Summary report: N

UNKNOWN

MDR report key: 9640622 · Received January 29, 2020

Report

Report Number
3002808486-2020-00113
Event Type
Injury
Date Received
January 29, 2020
Report Date
January 28, 2020
Manufacturer
WILLIAM COOK EUROPE
Product Code
DTK
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

MANUFACTURER REF# (B)(4). CATALOG# IS UNKNOWN BUT REFERRED TO AS COOK CELECT PLATINUM FILTER. OCCUPATION: NON-HEALTHCARE PROFESSIONAL. PMA/510(K) K171712. IT HAS NOT BEEN POSSIBLE TO INVESTIGATE OR EVALUATE THIS ALLEGED EVENT BASED ON THE LIMITED INFORMATION PROVIDED TO DATE. COOK WILL REOPEN ITS INVESTIGATION IF FURTHER INFORMATION IS RECEIVING WARRANTING SUPPLEMENTATION IN ACCORDANCE WITH 21 C.F.R. 803.56.

Description of Event or Problem · 1

DESCRIPTION OF EVENT ACCORDING TO SHORT FORM COMPLAINT FILED: IT IS ALLEGED THAT "[PT] RECEIVED A COOK CELECT PLATINUM FILTER ON (B)(6) 2015. IT IS ALLEGED THAT THE [PT] WAS INJURED WITHOUT FURTHER EXPLANATION. HOSPITAL AND MEDICAL RECORDS HAVE BEEN REQUESTED BUT NOT YET PROVIDED."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
104383 UNKNOWN DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR DTK WILLIAM COOK EUROPE UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Life Threatening