United StatesPlum Solo Precision IV Pump (40001-0401), Plum Duo Infusion Pump (40002-0401) and Plum Duo Precision IV Pump (40002-0403) distributed worldwide including US states ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and Canada are affected. Under certain conditions the pump may not display a soft limit alert and will not notify the clinician of a soft limit violation before confirming and starting delivery, which may potentially lead to under- or over-delivery.
What's being recalled
Plum Solo Precision IV Pump, 40001-0401
Plum Duo Infusion Pump, 40002-0401
Plum Duo Precision IV Pump, 40002-0403
Recalling firm: ICU Medical, Inc., Lake Forest, IL, United States.
How to identify it
UDI-DI M335400011 Plum Solo Precision IV Pump v1.0.3 UDI-DI M335400021 Plum Duo Infusion Pump v1.2.3 UDI-DI M335400031 Plum Duo Precision IV Pump v1.2.3
The hazard
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
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 ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.
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)
Canada