FDA Device recall Z-2734-2014
The Rejuvenator Chamber manufactured by Baro-Therapies, Inc
- FDA Device
- Class II
- terminated
- Published 2014-10-08
On 2014-10-08 the FDA classified a Class II recall of The Rejuvenator Chamber manufactured by Baro-Therapies, Inc by Baro Therapies, citing the firm is distributing the Rejuvenator device without an approved 510(k).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2734-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-08 |
| Published | 2014-10-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baro Therapies |
| Distribution | US |
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.
Reason
The firm is distributing the Rejuvenator device without an approved 510(k).
Identifiers
| code_info | All Lots, Series and Codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2734-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.