- Recalling firm
- Medtronic Perfusion Systems
- Reason for recall
- Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
- Affected products (lot / model / serial)
- MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220
- Distribution pattern
- Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
- Firm location
- Brooklyn Park, MN, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2738-2026
- Recall initiated
- May 25, 2026
- FDA classification date
- July 15, 2026
- FDA report date
- July 22, 2026
- FDA event ID
- 99199
- Last updated on HTM Vibe
- July 28, 2026