FDAFDA · Food and drugs·Recall number Z-2580-2026
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Published July 1, 2026 · Recall initiated: May 11, 2026
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
What to do
Voluntary: Firm initiated · Visit
Recall details
- Manufacturer
- Boston Scientific Corporation
- Distributor
- US Nationwide distribution in the state of OH.
- Lot
- GTIN 00850014110147, Serial Number 20175
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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