Boston Scientific Corporation recalls Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP
See all recalls from Boston Scientific Corporation →Recalled Product
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Hazard / Issue
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: GTIN 00850014110147, Serial Number 20175
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Intera Oncology INTERA 3000 →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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