Agiliti Health Recalls Adapt Pump Support Surfaces Due to Software Malfunction
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Agiliti Health is recalling 4,286 Adapt Pumps used in medical support surfaces because a software bug prevents the Microclimate Management function from restarting after an Autofirm cycle.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 6, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Agiliti Health - Ellis has initiated a voluntary Class II recall of its Adapt Pump (Model 61600200) used with several medical support surfaces. The company identified a software defect where the Microclimate Management function fails to re-engage after the "Autofirm" function's 10-minute timer elapses. This issue occurs specifically when the timer is allowed to run out after the initial setup and affects only the Microclimate Management function.
Which Products Are Affected
The recall affects 4,286 units distributed nationwide across the United States. Affected products include:
- Product Name: Adapt Pump (Component of Adapt support surfaces including Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, and Adapt Convertible EX)
- Model/Catalog Number: 61600200
- Software Version: 1.3.0
- Identification: UDI-DI 0084569904914. This recall includes all serial numbers with a manufacturing date prior to December 4, 2025.
What You Should Do
Agiliti Health initiated the notification process via email on January 21, 2026. Facilities and healthcare providers using these support surfaces should be aware that the Microclimate Management function may not automatically resume after using the Autofirm setting. For more information regarding the status of the recall or technical support, contact Agiliti Health - Ellis at their 204 W 2nd St location in Ellis, Kansas.
Why This Matters
The failure of the Microclimate Management function to re-engage could compromise the therapeutic environment provided by the air flotation and alternating pressure mattresses, potentially impacting patient care.
Source
Information provided by the FDA under recall number Z-1472-2026.
Original source: FDA Official Notice ↗
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