Baro-Therapies, Inc: Medical Device Recall in 2014 - (Recall #: Z-2734-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: August 8, 2014

Date Posted: October 8, 2014

Recall Number: Z-2734-2014

Event ID: 69053

Reason for Recall:

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

Status: Terminated

Product Quantity: 10

Code Information:

All Lots, Series and Codes

Distribution Pattern:

US Nationwide Distribution in the states of FL, GA, MS, TN and CO.

Voluntary or Mandated:

Voluntary: Firm initiated