United StatesMedtronic DLP One‑Piece Pediatric Arterial Cannula (Product Number/CFN 77010; MATNR A7630009466801/UDI/DI 20763000946689; Lot 0231650870) and Medtronic Bio‑Medicus Adult Cannula Kit (Product Number/CFN 96530‑115; MATNR 00763000116019/UDI/DI 00643169769076; Lot 230257001) are being recalled by Medtronic Perfusion Systems. The recall follows two complaints of loose foreign material confirmed as containing trace levels of blood; these cardiopulmonary bypass vascular cannulae were distributed worldwide, including US states MD, CA, MI, WA, PA, NC, FL and AR.
What's being recalled
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula
Recalling firm: Medtronic Perfusion Systems, Brooklyn Park, MN, United States.
How to identify it
MATNR A7630009466801/UDI/DI 20763000946689, Lot Numbers: 0231650870, C232227220 MATNR 00763000116019/UDI/DI 00643169769076, Lot Number: 230257001
The hazard
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide - US Nationwide distribution in the states of MD, CA, MI, WA, PA, NC, FL, AR.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)