[Recalled] 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 pro
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | 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. |
|---|---|
| Brand / manufacturer | Covidien LP |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1469-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 May 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Covidien LP
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.