Class II — Potential Health Hazard

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

The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by Baro-Therapies, Inc Due to The firm is distributing the Rejuvenator device without...

Date: August 8, 2014
Company: Baro-Therapies, 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 Baro-Therapies, Inc directly.

Affected Products

The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and pains brought on by changes in the weather.

Quantity: 10

Why Was This Recalled?

The firm is distributing the Rejuvenator device without an approved 510(k).

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Baro-Therapies, Inc

Baro-Therapies, Inc has 1 total recall tracked by RecallDetector.

Related Recalls

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