← FDA ENFORCEMENT
Z-2738-2026Class II

Medtronic Perfusion Systems

Recalling firm
Medtronic Perfusion Systems
Product type
Device
Status
Ongoing
Report date
2026-07-22
Distribution
Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
Firm state
MN
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

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

Product description

Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula

Code / lot info

MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220

Other recalls SPEQ maps to Environmental Monitoring
2026-07-22Class IFrutas y Hortalizas del Sur S.A.2026-07-22Class IIGELLERT GLOBAL GROUP2026-07-22Class IICareFusion 213, LLC2026-07-22Class IIChiesi USA, Inc.
See all Environmental Monitoring recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.