Covidien LP: Medical Device Recall in 2013 - (Recall #: Z-1469-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product Code: ONB5STF 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.

Product Classification:

Class II

Date Initiated: May 6, 2013

Date Posted: June 12, 2013

Recall Number: Z-1469-2013

Event ID: 65093

Reason for Recall:

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

Status: Terminated

Product Quantity: 126925 units

Code Information:

Lot Numbers: N2H0353X through N3D0033X 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 Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated