Life Force Chamber Product Usage:The product is intended for restful… — Class II medical device recall Z-2625-2014
Terminated recall by Life Force of Tampa, LLC, reported 2014-09-17, distributed nationwide. The Life Force chamber is marketed and promoted as a medical device, intended for use in the diagnosis of dise
| Recall number | Z-2625-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Life Force of Tampa, LLC, Tampa, FL, United States |
| Recall initiated | 2014-06-27 |
| Classified | 2014-09-11 |
| Reported by FDA | 2014-09-17 |
| Terminated | 2015-07-30 |
| Distributed | Nationwide (US) |
| Quantity | 10 |
Product
Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
Reason for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2625-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.