Notice names this product. Medtronic Perfusion Systems’s Medtronic DLP One-Piece Pediatric Arterial Cannula is named in FDA Class II recall Z-2738-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood. Identifying details: MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220. Status: Ongoing.
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.
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; 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.
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Company / brand: Medtronic Perfusion Systems
Affected product: Medtronic DLP One-Piece Pediatric Arterial Cannula
Official ID Z-2738-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.