FDA recall, , Moderate risk
Agiliti Adapt Pump
The Adapt Pump may not re-engage the Microclimate Management function after using Autofirm for 10 minutes.
Summary by Recall Canary from the FDA notice
What happened
Agiliti Health - Ellis, in Ellis, Kansas, recalled the Adapt Pump, a component of Adapt support surfaces including Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, and Adapt Convertible EX. The company identified an issue where the pump does not re-engage the Microclimate Management function after using the Autofirm function for 10 minutes.
This issue occurs only when the 10-minute timer elapses after the Autofirm button is pressed after initial setup, and it affects only the Microclimate Management function. The recall began January 21, 2026, and was added to the FDA's Enforcement Report on February 26, 2026. Distribution was nationwide in the US.
The pump is an air flotation mattress with alternating pressure. The recall was classified by the FDA on February 26, 2026, and included in the FDA's weekly enforcement report on March 4, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Adapt Pump
- Other code
- 0084569904914
- Model number
- 61600200-Adapt Pump
- Lot code
- All serial numbers with a manufacturing date prior to 12/04/2025
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Agiliti Health - EllisEllis, Kansas
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98332
- Recall number
- Z-1472-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
