Stryker Corporation recalls This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contain

Recalled July 10, 2024 · FDA recall Z-2261-2024 · Stryker

Hazard

Expired Products distributed to customers · FDA Class II

Units

8 units

Sold at

US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.

Description

Expired Products distributed to customers

Product

This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225

Manufacturer(s)

Stryker Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →