# FDA recall Z-1472-2026

> **Agiliti Health - Ellis** · Class II · device recall initiated 2026-01-21.

## 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

## Reason for recall

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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1472-2026
- **Recalling firm:** Agiliti Health - Ellis
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-21
- **Report date:** 2026-03-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ellis, KS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1472-2026

## Citation

> AI Analytics. FDA recall Z-1472-2026. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-1472-2026. Source: US FDA. Licensed CC0.

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