FDA recall Z-2261-2024

Stryker Corporation · Class II · device

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

Reason for recall

Expired Products distributed to customers

Distribution

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

Key facts

Status
Ongoing
Initiation date
2024-06-03
Report date
2024-07-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Portage, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2261-2024