Z-2261-2024 Class II Ongoing

Recalled by Stryker Corporation — Portage, MI

Recall Details

Product Type
Devices
Report Date
July 10, 2024
Initiation Date
June 3, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
8 units

Product Description

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

Reason for Recall

Expired Products distributed to customers

Distribution Pattern

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

Code Information

GTIN: 07613327118438 Lot Number: 1000388946