FDA Adverse Event Injury Summary report: N

*

MDR report key: 480288 · Received August 26, 2003

Report

Report Number
2515651-2003-00004
Event Type
Injury
Date Received
August 26, 2003
Date of Event
May 1, 2003
Manufacturer
PILLING SURGICAL
Product Code
KBN
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * KBN PILLING SURGICAL * *

Patients

Seq Age Sex Outcome Treatment
1