United StatesMedtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03, UDI/DI 20763000433844, Lot 232135734 (3850 units) distributed in the United States to Hawaii and New York may be affected. The lot was recalled after Medtronic personnel observed trace amounts of dry blood on the external carton label and on the Instructions for Use in five boxes of that lot.
What's being recalled
Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03
Recalling firm: Medtronic Perfusion Systems, Brooklyn Park, MN, United States.
How to identify it
UDI/DI 20763000433844, Lot Number 232135734
The hazard
Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges.
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
US Nationwide distribution in the states of Hawaii and New York.
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)