Intera Oncology INTERA 3000 Hepatic Artery Infusion recall
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Why was Intera Oncology INTERA 3000 Hepatic Artery Infusion recalled?
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
GTIN 00850014110147, Serial Number 20175
- Product
- Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
- Recalling firm
- Boston Scientific Corporation
- Quantity
- 1 device
- Distribution
- US Nationwide distribution in the state of OH.
- Recall date
- July 1, 2026
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)