Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Pressure IQ Evolve Mattress Recalled by Arjo Hospital Equipment AB Due to The firm received complaints regarding multiple mattresses were...

Date: September 1, 2014
Company: Arjo Hospital Equipment AB
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Arjo Hospital Equipment AB directly.

Affected Products

Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers while on a mattress.

Quantity: 1,034 units

Why Was This Recalled?

The firm received complaints regarding multiple mattresses were showing failures resulting in pressure ulcers.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Arjo Hospital Equipment AB

Arjo Hospital Equipment AB has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report