Class II

Medical Device Recall: Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD

Covidien · November 16, 2023

Reason for Recall

Due to software issue, New systems may exhibit an error which may prohibit use of new systems resulting in system being inoperable

Distribution

Worldwide distribution - US: Nationwide and surrounding territories.

States Affected

NATIONWIDE

Quantity Affected

47,901 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0631-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.