Class II

Medical Device Recall: Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

Boston Scientific Corporation · May 11, 2026

Reason for Recall

There is the potential for leakage along the drug pathway from the pump through the end of the catheter.

Distribution

US Nationwide distribution in the state of OH.

States Affected

NATIONWIDE

Quantity Affected

1 device

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2580-2026

Status: completed

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.