Fresh Recalls

FDAClass II · Medical device · Recall Z-2580-2026 · Recalled July 1, 2026

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

Agency report date: July 1, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump
Company / brand
Boston Scientific
Lot / serial / date codes
GTIN 00850014110147, Serial Number 20175
Distribution
US Nationwide distribution in the state of OH.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump

3. Open the official notice or contact

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

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
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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