United StatesThe Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump (AP-0300H), an implantable drug delivery device (GTIN 00850014110147, Serial Number 20175), is affected. It was recalled because of the potential for leakage along the drug pathway from the pump through the end of the catheter. The device was distributed in the United States, with distribution in the state of Ohio.
What's being recalled
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Recalling firm: Boston Scientific Corporation, Maple Grove, MN, United States.
How to identify it
GTIN 00850014110147, Serial Number 20175
The hazard
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the state of OH.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)
Canada