FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Medical device · Recalled July 1, 2026

Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall — Boston Scientific Corporation

Hazard: There is the potential for leakage along the drug pathway from the pump through the end of the catheter.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
Z-2580-2026
Brand
Boston Scientific
Classification
Class II
Units affected
1 device
Recall status
Completed
Initiated
Voluntary: Firm initiated

Description

Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

Affected products

Companies & origin

Recalling firm location
Maple Grove, MN, United States
Firm address
1 Scimed Pl, N/A, 55311-1565

Identifying details (verbatim from the notice)

Product codes / lots
GTIN 00850014110147, Serial Number 20175
Distribution
US Nationwide distribution in the state of OH.
Firm notified the public via
Visit
FDA event ID
99063
Recall initiated
May 11, 2026
FDA classified
June 25, 2026
FDA report date
July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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