Z-2403-2026Class II

Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10...

Name: Z-2403-2026 Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10...
Creator: Boston Scientific Neuromodulation Corporation
Published: 2026-04-29
License: https://open.fda.gov/license/

Boston Scientific Neuromodulation Corporation / initiated 2026-04-29 / Open, Classified

FDA source

Boston Scientific Neuromodulation Corporation began a recall of Boston 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... on 2026-04-29. FDA classified it as Class II and gives the reason as "Reusable electrodes may not meet expected performance levels". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-2403-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-04-29
Posted: 2026-06-11
Recalling firm: Boston Scientific Neuromodulation Corporation
Product: Boston 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 Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in); REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45 mm (0.0175 in) REF: TCN-5-3m, TCN Electrode, NITINOL, 3M CABLE, 5 cm x 0.45 mm (0.0175 in) REF: TCN-10-3M, TCN Electrode, NITINOL, 3M CABLE, 10 cm x 0.45 mm (0.0175 in); REF: TCN-15-3M, TCN Electrode, NITINOL, 3M CABLE, 15 cm x 0.45 mm (0.0175 in) REF: TCN-20-3M, TCN Electrode, NITINOL, 3M CABLE, 20 cm x 0.45 mm (0.0175 in)
Product code: GXI Probe, Radiofrequency Lesion
Reason for recall: Reusable electrodes may not meet expected performance levels.
FDA root cause: Under Investigation by firm
Action: 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.
Quantity in commerce: 49,251 units
Distribution: Worldwide distribution - US Nationwide and the countries of PE, MX, PR, CO, MY, CA.
Product codes and lots: All Lots: / UDI: TCN-10: 00813250013054; TCN-10-3M: 00813250017502; TCN-15: 00813250013061; TCN-15-3M: 00813250017519; TCN-20: 00813250013078; TCN-20-3M: 00813250017526; TCN-5: 00813250013047; TCN-5-3M:00813250017533

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2403-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2402-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-06-17	2026-06-11
Z-2403-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-06-17	2026-06-11

Product code GXI

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)