Medical Device Recall: 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 ins
Stryker Corporation · June 3, 2024
Reason for Recall
Expired Products distributed to customers
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
Distribution
US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
States Affected
NATIONWIDE
Quantity Affected
8 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2261-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.