agiliti health - ellismedicalHigh PriorityActive

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

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 was recalled because 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.. If you have this product, stop using it until you verify your lot or model details.

By RecallRadar Editorial Team

Sourced from FDA. Last verified March 15, 2026.

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Key facts

Date announced: March 4, 2026
Source agency: FDA

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

What's Being Recalled

Quoted source excerpt from the official notice.

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.

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand: Agiliti health - ellis
Category: medical
Source agency: FDA
Announced: March 4, 2026
Country: US
Status: Active

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

UDI-DI 0084569904914; All serial numbers with a manufacturing date prior to 12/04/2025

#	Model
1	UDI-DI 0084569904914; All serial numbers with a manufacturing date prior to 12/04/2025

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

1Stop using the affected product until you verify whether your item is impacted.
2Check the official recall notice and match your model, lot, or serial details.
3Follow the official instructions for repair, replacement, refund, or disposal.

Open Official Recall Notice

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: March 4, 2026
Last reviewed by RecallRadar: March 15, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists UDI-DI 0084569904914; All serial numbers with a manufacturing date prior to 12/04/2025.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the agiliti health - ellis recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-1472-2026&limit=1

Keep browsing with these internal hubs: agiliti health - ellis recall hub and Medical recall hub.