Official recall notice
FDA DeviceClass IINotable
FDA Recall: Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
- Recall date
- 2026-07-01
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
Product description
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
Affected products
GTIN 00850014110147, Serial Number 20175