FDA
Food and Drug Administration · Recall Z-2580-2026 · May 11, 2026Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Boston Scientific Corporation
The hazard
There is the potential for leakage along the drug pathway from the pump through the end of the catheter. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model GTIN 00850014110147Model Serial Number 20175UPC 00850014110147Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.