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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

Agiliti Adapt Pump Recalled for Microclimate Management Function Failure

Agency Publication Date: February 26, 2026
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Summary

Agiliti Health is recalling approximately 4,286 Adapt Pumps used with various Adapt Line support surfaces because a software issue prevents the Microclimate Management function from re-engaging. This failure occurs after the 'Autofirm' mode has been active for its 10-minute cycle and the timer is allowed to expire. The affected pumps were manufactured prior to December 4, 2025, and include software version 1.3.0.

Risk

If the Microclimate Management function fails to restart, the system may not effectively manage the patient's skin temperature and moisture levels, which can increase the risk of skin breakdown or pressure injuries. No specific injuries have been reported in the provided data.

What You Should Do

  1. Identify your device by checking the pump model number 61600200-Adapt Pump and looking for UDI-DI 0084569904914 on the product label.
  2. Check the manufacturing date and software version of your pump; this recall affects software version 1.3.0 and all serial numbers manufactured prior to December 4, 2025.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Adapt Pump (component of Adapt support surfaces: Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX)
Variants: Software version 1.3.0
Model / REF:
61600200-Adapt Pump
UDI:
0084569904914
Date Ranges: All manufacturing dates prior to 12/04/2025

Recall #: Z-1472-2026. Includes various Adapt support surfaces including Air, Air EX, Air Pro, Air Pro EX, Convertible, and Convertible EX.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98332
Status: Active
Manufacturer: Agiliti Health - Ellis
Sold By: Agiliti Health; Specialty medical distributors
Manufactured In: United States
Units Affected: 4286
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.