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Baro-Therapies, Inc recalls The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches
Recalled October 8, 2014 · FDA recall Z-2734-2014 · Baro-Therapies
Hazard
The firm is distributing the Rejuvenator device without an approved 510(k). · FDA Class II
Units
10
Sold at
US Nationwide Distribution in the states of FL, GA, MS, TN and CO.
Description
The firm is distributing the Rejuvenator device without an approved 510(k).
Product
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.
Manufacturer(s)
Baro-Therapies, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →