Reported Jun 12, 2013 · Terminated
Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Product Code: ONB5STF2C The Versaport" Bladeless…
Covidien LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Covidien LP · 60 Middletown Ave · North Haven, CT · 06473-3908
Is this the product you have?
- Versaport Bladeless Optical Trocar With (2)
- Fixation Cannulae - 5mm Product CodeONB5STF2C 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
- Lot codes and dates
- Lot NumbersN2J0211X
- through N3D0118X NoteThe specific lot numbers listed below are not affected by
- this recall and are acceptable for use
N2H0045XN2H0166XN2H0286XN2H0357XN2 H051 6UX
- Amount recalled
- 5364 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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