Notice names this product. Boston Scientific’s Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump is named in FDA Class II recall Z-2580-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: There is the potential for leakage along the drug pathway from the pump through the end of the catheter. Identifying details: GTIN 00850014110147, Serial Number 20175. Units affected: 1 device. Status: Completed.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
Company / brand: Boston Scientific
Affected product: Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump
Official ID Z-2580-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.