Boston Scientific CSK Electrodes recallZ-2402-2026 · Boston Scientific Neuromodulation Corporation · initiated Apr 29, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Boston Scientific Neuromodulation Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Reusable electrodes may not meet expected performance levels.
FDA root cause category: Under Investigation by firm
What the company is doing
On April 29, 2026, Boston Scientific issued a Urgent Medical device Removal Notification via Federal Express/email/hand delivery. Boston Scientific asked consignees to take the following actions: 1. DO NOT use affected product. Remove affected products from your facility s inventory, and segregate the units in a secure place. 2. For products already in use, immediately discard according to your facility s procedure. 3. Unused products should be returned to Boston Scientific in accordance with the enclosed instructions. 4. Immediately post this information in a visible location near the affected products to ensure this information is readily accessible to all handlers and users of the device. 5. Forward this notice to any healthcare professional from your organization for awareness and to any organization where affected devices have been transferred. 6. Complete and return the enclosed Reply Verification Tracking Form per the enclosed instructions.
Recall details
- Recall number
- Z-2402-2026
- Status
- Open, Classified
- Initiated by the company
- Apr 29, 2026
- Posted by the FDA
- Jun 11, 2026
- Recalling firm
- Boston Scientific Neuromodulation Corporation
- Quantity
- 31,923 units
- Product code
- GXI
- FDA submissions
- K050084, K183177
- Distribution
- Worldwide distribution - US Nationwide and the countries of PE, MX, PR, CO, MY, CA.
Product description
Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm); REF: CSK-TC15, CSK Electrode, STAINLESS STEEL, 15 cm x 28 ga (0.36 mm); REF: CSK-TC15-3M, CSK Electrode, STAINLESS STEEL, 3M Cable, 15 cm x 28 ga (0.36 mm) REF: CSK-TC20, CSK Electrode, STAINLESS STEEL, 20 cm x 28 ga (0.36 mm) REF: CSK-TC5,CSK Electrode, STAINLESS STEEL, 5 cm x 28 ga (0.36 mm); REF: CSK-TC5-3M, CSK Electrode, STAINLESS STEEL, 3M Cable, 5 cm x 28 ga (0.36 mm)
Code information (models, lots, serial numbers)
All Lots: / UDI: CSK-TC10:00813250010107; CSK-TC10-3M: 00813250011524; CSK-TC15 00813250010114; CSK-TC15-3M: 00813250011548 CSK-TC20: 0081325001140; CSK-TC5: 00813250010091; CSK-TC5-3M: 00813250011531;
Devices named in this recall
6 devices in the FDA device registry whose identifier appears in the recall's code information.
- NA CSK-TC10Boston Scientific Neuromodulation Corporation · PROBE, RADIOFREQUENCY LESION1 recall1 death58 reports
- NA CSK-TC10-3MBoston Scientific Neuromodulation Corporation · GENERATOR, LESION, RADIOFREQUENCY1 recall34 reports
- NA CSK-TC15Boston Scientific Neuromodulation Corporation · GENERATOR, LESION, RADIOFREQUENCY1 recall22 reports
- NA CSK-TC15-3MBoston Scientific Neuromodulation Corporation · GENERATOR, LESION, RADIOFREQUENCY1 recall7 reports
- NA CSK-TC5Boston Scientific Neuromodulation Corporation · PROBE, RADIOFREQUENCY LESION1 recall3 reports
- NA CSK-TC5-3MBoston Scientific Neuromodulation Corporation · PROBE, RADIOFREQUENCY LESION1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 98939).
- Z-2403-2026 · Open, ClassifiedBoston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN El…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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