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
- Company
- Stryker Corporation
- Recall Initiated
- June 3, 2024
- Posted
- July 3, 2024
- Recall Number
- Z-2261-2024
- Quantity
- 8 units
- Firm Location
- Portage, MI
Reason for Recall
Expired Products distributed to customers
Distribution
US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
Lot / Code Info
GTIN: 07613327118438 Lot Number: 1000388946
Root Cause
Storage
Action Taken
Stryker issued Urgent Medical Device Recall Letter on 6/3/24 via Fed'X. Letter states reason for recall, health risk and action to take: Actions to be taken: 1. Immediately check your inventory to locate and quarantine any affected products found at your facility. 2. Sign and return the enclosed Business Response Form (BRF) by email to Instruments.recalls@stryker.com, even if affected product is no longer in your inventory. 3. Upon receipt of the completed BRF, a shipping label will be provided to return any recalled product on-hand and Stryker will arrange for replacement product(s) to be shipped promptly. 4. Maintain awareness of this communication internally and inform Stryker if any of the devices have been distributed to other organizations. If so, provide contact details so Stryker can inform the recipients accordingly. Please contact Lacey Marshall at 269-270-5950 or Instruments.recalls@stryker.com with questions or concerns.