FDA Adverse Event Injury Summary report: N

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

MDR report key: 5665632 · Received May 19, 2016

Report

Report Number
3002808486-2016-00280
Event Type
Injury
Date Received
May 19, 2016
Report Date
May 3, 2016
Manufacturer
COOK INC
Product Code
DTK
PMA / PMN Number
K090140
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

MANUFACTURER REF# (B)(4). CATALOG#: UNKNOWN BUT REFERRED TO AS A COOK GÜNTER TULIP FILTER. EXPIRATION DATE: UNKNOWN AS LOT# IS UNKNOWN. INVESTIGATION IS STILL IN PROGRESS.

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION PROVIDED ON 16JAN2017 DETERMINED THAT THIS DEVICE WAS MANUFACTURED BY COOK INC. WITH THE SUBMISSION OF THIS FOLLOW UP REPORT, WILLIAM COOK EUROPE INFORMS THAT THIS COMPLAINT HAS BEEN TRANSFERRED FROM WILLIAM COOK EUROPE TO COOK INC. COOK INC. WILL HANDLE THIS EVENT UNDER REFERENCE# 1820334-2017-00153 FOR ALL FUTURE REPORTS TO FDA. (B)(4). INVESTIGATION IS STILL IN PROGRESS.

Description of Event or Problem · 1

DESCRIPTION ACCORDING TO SHORT FORM COMPLAINT FILED: IT IS ALLEGED THAT "[PT] RECEIVED A COOK GUNTHER TULIP FILTER ON (B)(6) 2009 AT (B)(6)". PATIENT OUTCOME: IT IS ALLEGED THAT [PT] WAS INJURED WITHOUT FURTHER EXPLANATION. HOSPITAL AND MEDICAL RECORDS HAVE BEEN REQUESTED BUT NOT YET PROVIDED.

Description of Event or Problem · 1

DESCRIPTION ACCORDING TO SHORT FORM COMPLAINT FILED: IT IS ALLEGED THAT "[PT] RECEIVED A COOK GUNTHER TULIP FILTER ON (B)(6) 2009." PATIENT OUTCOME: IT IS ALLEGED THAT [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
321369 GUNTHER TULIP JUGULAR VENA CAVA FILTER SET DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR DTK COOK INC

Patients

Seq Age Sex Outcome Treatment
1 Life Threatening| O