Olympus Corporation of the Americas: Medical Device Recall in 2022 - (Recall #: Z-0424-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S

Product Classification:

Class II

Date Initiated: November 4, 2022

Date Posted: December 14, 2022

Recall Number: Z-0424-2023

Event ID: 91100

Reason for Recall:

An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of the surgical procedure.

Status: Ongoing

Product Quantity: 186 boxes (930 pieces)

Code Information:

Model Number/ UDI-DI/ Lot Number WA22602S 14042761085127 1000090824 WA22603S 14042761085134 1000092201 WA22621S 14042761085172 1000080316 WA22657S 14042761085301 1000092202

Distribution Pattern:

US Nationwide domestic distribution.

Voluntary or Mandated:

Voluntary: Firm initiated