FDA-Device2024-07-10Class II
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
Stryker Corporation
Hazard
Expired Products distributed to customers
Sold states
US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
Affected count
8 units
Manufactured in
1941 Stryker Way, N/A, Portage, MI, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2261-2024Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief