Covidien: Medical Device Recall in 2024 - (Recall #: Z-0631-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 16, 2023

Date Posted: January 10, 2024

Recall Number: Z-0631-2024

Event ID: 93561

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

Status: Ongoing

Product Quantity: 47,901 units

Code Information:

Ref-UDI: VLFT10GEN- 10884521516328, DLVLFT10GEN - 10884521787056 , VLFT10GENZD - 10884521640474/Software: v4.0.1, v4.0.2 and v4.0.3

Distribution Pattern:

Worldwide distribution - US: Nationwide and surrounding territories.

Voluntary or Mandated:

Voluntary: Firm initiated