Z-2261-2024 Class II Ongoing
FDA device recall Z-2261-2024 was initiated by Stryker Corporation on Jun 3, 2024 and is designated Class II. Reason for recall: Expired Products distributed to customers The recall status is ongoing. Affected quantity: 8 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 10, 2024
- Initiation Date
- Jun 3, 2024
- 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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2261-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026