Covidien Llc recalls Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081…

Recall date

February 10, 2020

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1446-2020

FDA classification

Class II

Brand / firm

Covidien Llc

Sold / distributed

Nationwide domestic distribution. Foreign distribution to Australia, Canada, Austria Belgium Canary Islands Czech Republic Denmark Finland France Germany Greece Hungary Italy Jordan Kazakhstan Kenya Lithuania Luxembourg North Macedonia Poland Portugal Reunion Romania Russian Federation Serbia Slova…

Why it was recalled

Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934