United StatesThe Adapt Pump (Model/Catalog 61600200), a component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX) running software version 1.3.0 and used with alternating pressure mattresses, is being recalled; affected units include UDI-DI 0084569904914 and all serial numbers with a manufacturing date prior to 12/04/2025 (4,286 units distributed nationwide in the U.S.). Agiliti found the pump may not re‑engage the Microclimate Management function after using the Autofirm function for 10 minutes when the 10‑minute timer elapses, and the issue only affects that function.
What's being recalled
Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware version 1.3.0; Mattress, Air Flotation, Alternating Pressure
Recalling firm: Agiliti Health - Ellis, Ellis, KS, United States.
How to identify it
UDI-DI 0084569904914; All serial numbers with a manufacturing date prior to 12/04/2025
The hazard
Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate Management function after using the Autofirm function for 10 minutes. This issue only occurs when the 10-minute timer is allowed to elapse after the Autofirm button is pressed after initial setup, and it only affects the Microclimate Management function.
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.
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)