Vortex Surgical Inc.: Medical Device Recall in 2024 - (Recall #: Z-0970-2024)

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:

Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25

Product Classification:

Class II

Date Initiated: December 18, 2023

Date Posted: February 7, 2024

Recall Number: Z-0970-2024

Event ID: 93725

Reason for Recall:

Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.

Status: Terminated

Product Quantity: 800 devices

Code Information:

UDI/DI 00810123481132, Lot Numbers 2212002 and 2212020

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and the country of Republic of Korea

Voluntary or Mandated:

Voluntary: Firm initiated