FDA Enforcement Class II Terminated

Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST The Versaport" Bladeless Optical 5mm trocars are intended for use in a variety of gynecologic, general, thoracic and urologic endoscopic procedures to create and maintain a port of entry.

Recall: Z-1472-2013 · Reported June 12, 2013

Enforcement

Recall Number
Z-1472-2013
Event ID
65093
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Covidien LP
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 12, 2013
Initiation Date
May 6, 2013
Classification Date
June 5, 2013
Termination Date
August 12, 2014
Address
60 Middletown Ave, N/A, North Haven, CT, 06473-3908, United States

Description

Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST The Versaport" Bladeless Optical 5mm trocars are intended for use in a variety of gynecologic, general, thoracic and urologic endoscopic procedures to create and maintain a port of entry.

Reason

Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity

Code Info

Lot Numbers: N2J0150X through N3C0683X Note: The specific lot numbers listed below are not affected by this recall and are acceptable for use: N2H0045X,N2H0166X,N2H0286X, N2H0357X,N2 H051 6UX

Distribution

Worldwide Distribution - USA (nationwide) and internationally to the following countries: Canada Austria Bahrain Benoni Centurion Chatsworth Czech Republic Denmark Egypt Finland France Germany Ireland Israel Italy Japan Kuwait Netherlands Norway Portugal QATAR Saudi Arabia Serbia Singapore South Africa Spain OMAN Sweden Switzerland UAE United Kingdom Venezuela

Quantity

57461 untis