Intera 3000 Hepatic Artery Pump Recall: Higher Flow Rate Risk

Take action

Contact the company & request your remedy

Recalling firmIntera Oncology, Inc.65 William St · Wellesley, MA 02481-3802

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Intera Oncology is recalling its INTERA 3000 Hepatic Artery Infusion Pumps due to a higher than expected flow rate that could cause complications. This is a serious medical device that patients use for chemotherapy treatments.

Why it’s dangerous

The pump may deliver medication too quickly, causing dangerous blood flow rates. This could lead to complications like tissue damage or other serious health issues during chemotherapy treatment.

Who’s affected

Patients using the INTERA 3000 Hepatic Artery Infusion Pump for chemotherapy treatments are most at risk. The device is implanted and used for specific medical procedures.

How to tell if you have this one

Check the serial number on your pump. Affected units have specific serial numbers listed in the recall notice. The pump is an implantable device used for chemotherapy treatments.

Brand
Intera
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Look for the serial number on your pump to see if it matches the list of affected units provided in the recall.

✎ GovInfoNow

Questions people ask

Is this pump safe to use?

The recall states there is a higher than expected flow rate, which could cause complications. Do not use until you check the serial number and follow the action steps.

What should I do if I have this pump?

Check the serial number against the list of affected units. If it matches, stop using the pump and contact Intera Oncology for further instructions.

How can I get a replacement?

The recall does not specify a remedy. Contact Intera Oncology directly for assistance with replacement or repair options.

Take action

Contact Intera

We’ve drafted a message you can send Intera to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1522-2022 — Intera Intera

Hello,

I own a Intera that is covered by recall Z-1522-2022 from Intera.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1522-2022 (July 10, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1522-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Intera Oncology, Inc. recalls INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.

Use caution until it’s fixed