Boston Scientific recalls Intera 3000 Hepatic Artery Infusion Pump AP-0300H due to potential drug leakage from the pump through the catheter. Affected units have specific serial numbers and GTIN.
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
Boston Scientific is recalling the Intera 3000 Hepatic Artery Infusion Pump (AP-0300H) because it may leak medication through the catheter. This could lead to improper drug delivery or exposure to the patient. The recall affects specific units with the serial number 20175 and GTIN 00850014110147.
The pump may leak medication along the drug pathway from the pump through the end of the catheter. This could cause improper drug delivery to the patient or expose them to medication in unintended areas. The risk is not described as causing serious injury in normal use.
Patients using the Intera 3000 Hepatic Artery Infusion Pump (AP-0300H) with serial number 20175 or GTIN 00850014110147 are affected. Healthcare providers administering this device are most at risk of potential medication exposure.
Check for the serial number 20175 or GTIN 00850014110147 on the pump. The product is an implantable drug delivery device used for hepatic artery infusion therapy.
Verify the serial number on the pump; affected units have serial number 20175.
The recall states there is a potential for leakage but does not specify it causes serious injury in normal use.
Check for the serial number 20175 or GTIN 00850014110147 on the pump.
The recall does not provide a remedy, so no action is required beyond checking the serial number.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2580-2026 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-2580-2026 from Boston Scientific. 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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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.
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