Stryker Corporation: Medical Device Recall in 2024 - (Recall #: Z-2261-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

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

Product Classification:

Class II

Date Initiated: June 3, 2024

Date Posted: July 10, 2024

Recall Number: Z-2261-2024

Event ID: 94755

Reason for Recall:

Expired Products distributed to customers

Status: Ongoing

Product Quantity: 8 units

Code Information:

GTIN: 07613327118438 Lot Number: 1000388946

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated