FDA Adverse Event Injury Summary report: N

0123680-COMPOSIX MESH E/X

MDR report key: 376439 · Received February 7, 2002

Report

Report Number
1213643-2002-00008
Event Type
Injury
Date Received
February 7, 2002
Date of Event
January 22, 2002
Report Date
February 7, 2002
Manufacturer
C.R. BARD, INC. (PUERTO RICO)
Product Code
FTL
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

BOWEL OBSTRUCTION 3 DAYS POST-OP EPTFE LAYER APPEARED TO HAVE PULLED AWAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 0123680-COMPOSIX MESH E/X 350101104-MESH COMPOSIX FTL C.R. BARD, INC. (PUERTO RICO) * UNK

Patients

Seq Age Sex Outcome Treatment
1 * Required Intervention