Adapt Pump Medical Device Recalled Due to Microclimate Management Function Failure
Agiliti Health - Ellis is recalling Adapt Pumps (Model 61600200) because the Microclimate Management function may fail to re-engage after using the Autofirm function.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which according to the rubric corresponds to a Moderate severity level.
Plain-English summary
Agiliti Health - Ellis has identified an issue with the Adapt Pump (Model/Catalog Number: 61600200-Adapt Pump), which is a component of Adapt support surfaces including the Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, and Adapt Convertible EX.
When the Autofirm function is used, the Microclimate Management function may fail to re-engage if the 10-minute timer is allowed to elapse after the Autofirm button is pressed following initial setup. This issue specifically affects the Microclimate Management function.
This recall affects 4,286 units with serial numbers manufactured prior to 12/04/2025. These products were distributed nationwide in the US.
The recalled product
- Product
- 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
- Manufacturer
- Agiliti Health - Ellis
- Hazard
- function-failure
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- UDI-DI 0084569904914
- All serial numbers with a manufacturing date prior to 12/04/2025
Distribution
Distributed nationwide across the United States.
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