Boston Scientific Corporation recalls Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump
- Recalling company
- Boston Scientific Corporation
- Product
- Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
- Reason
- There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 11, 2026
- Reported
- Jul 1, 2026
- Distribution
- US Nationwide distribution in the state of OH.
- Status
- Completed
- Quantity
- 1 device
- Lot / codes
- GTIN 00850014110147, Serial Number 20175
- Company location
- Maple Grove, MN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2580-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2580-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.