Official recall notice
FDA DeviceClass IINotable
FDA Recall: Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass
- Recall date
- 2026-07-22
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Product description
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Affected products
MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220