Class II — Potential Health Hazard

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

ActiveAid 922 Recalled by Altimate Medical, Inc. Due to Device manufactured with a component with affects the...

Date: November 30, 2022
Company: Altimate Medical, Inc.
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 Altimate Medical, Inc. directly.

Affected Products

ActiveAid 922, Shower/Commode Chair

Quantity: 1 unit

Why Was This Recalled?

Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Altimate Medical, Inc.

Altimate Medical, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

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