[Recalled] Covidien Duet TRS 60 4.8 mm Universal Articulating Single Use Loading Unit. Product Code: DUET6048A. Single Use Loading Unit (SULU) tissue reinforcement stapler. The Endo GIA Universal Staplers with Duet TRS reloads have appl
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Covidien Duet TRS 60 4.8 mm Universal Articulating Single Use Loading Unit. Product Code: DUET6048A. Single Use Loading Unit (SULU) tissue reinforcement stapler. The Endo GIA Universal Staplers with Duet TRS reloads have applications in abdominal, gynecologic and pediatric surgery for resection, |
|---|---|
| Brand / manufacturer | Covidien LP |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2439-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 21 August 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Duet TRS may have the potential to injure adjacent anatomical structures which may result in life threatening post-operative complications.
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.
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