Recalls / —
—#208195
Product
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
- FDA product code
- GXI — Probe, Radiofrequency Lesion
- Device class
- Class 2
- Medical specialty
- Neurology
- 510(k) numbers
- K032406
- Affected lot / code info
- GTIN: 07613327118438 Lot Number: 1000388946
Why it was recalled
Expired Products distributed to customers
Root cause (FDA determination)
Storage
Action the firm took
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.
Recalling firm
- Firm
- Stryker Corporation
- Address
- 1941 Stryker Way, Portage, Michigan 49002-9711
Distribution
- Distribution pattern
- US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
Timeline
- Recall initiated
- 2024-06-03
- Posted by FDA
- 2024-07-03
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #208195. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.