FDA Device recall Z-2625-2014
Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality
- FDA Device
- Class II
- terminated
- Published 2014-09-17
On 2014-09-17 the FDA classified a Class II recall of Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality by Life Force, citing the Life Force chamber is marketed and promoted as a medical device, intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment, or pre….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2625-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-27 |
| Published | 2014-09-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Life Force |
| Distribution | US |
Product
Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
Reason
The Life Force chamber is marketed and promoted as a medical device, intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment, or prevention of disease, or is intended to affect the structure or function of the body. Life Force of Tampa does not have an approved application for premarket approval in effect, or an approved application for an investigat
Identifiers
| code_info | ALL Life Force Chambers |
|---|
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-2625-2014%22
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