FDA Adverse Event Injury Summary report: N

PROTEKT

MDR report key: 1730061 · Received June 18, 2010

Report

Report Number
1651405-2010-00001
Event Type
Injury
Date Received
June 18, 2010
Date of Event
March 1, 2010
Report Date
March 31, 2010
Manufacturer
DIAMATRIX LTD
Product Code
HNN
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

NURSE CUT FINGER WHEN HAND SLIPPED TRYING TO CLOSE KNIFE SHEATH REQUIRING SUTURES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROTEKT SURGICAL KNIFE HNN DIAMATRIX LTD

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention