Fresh Recalls

FDAClass II · Medical device · Recall Z-2739-2026 · Recalled July 22, 2026

Medtronic Bio-Medicus Adult Cannula Kit recall — Medtronic Perfusion Systems

Agency report date: July 22, 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
Medtronic Bio-Medicus Adult Cannula Kit
Company / brand
Medtronic Perfusion Systems
Lot / serial / date codes
MATNR 00763000116019/UDI/DI 00643169769076, Lot Number: 230257001
Distribution
Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
Agency product description and boundaries

Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula

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: Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

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: Medtronic Bio-Medicus Adult Cannula Kit

3. Open the official notice or contact

Official recall ID
Z-2739-2026
Brand
Medtronic Perfusion Systems
Classification
Class II
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Brooklyn Park, MN, United States
Firm address
7611 Northland Dr N, 55428-1088

Identifying details (verbatim from the notice)

Product codes / lots
MATNR 00763000116019/UDI/DI 00643169769076, Lot Number: 230257001
Distribution
Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
Firm notified the public via
Letter
FDA event ID
99199
Recall initiated
May 25, 2026
FDA classified
July 15, 2026
FDA report date
July 22, 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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