Quick Facts at a Glance
- Recall Date
- May 11, 2026
- Hazard Level
- HIGH
- Brand
- Boston Scientific
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Boston Scientific
- Model numbers
- GTIN 00850014110147, Serial Number 20175
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 11, 2026
Reported by FDA DEVICE
July 1, 2026
RecallRadar source check
July 8, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Boston Scientific Corporation or your healthcare provider for instructions. Notification method: Visit
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Full Description
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. Quantity: 1 device. Distribution: US Nationwide distribution in the state of OH.
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: How to Get Refunds and ReplacementsWant to Know First?
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