FDA Medical Device Recalls (openFDA)
Life Force of Tampa, LLC: Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
- Recall number
- Z-2625-2014
- Recalling firm
- Life Force of Tampa, LLC
- Product
- Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
- Status
- Terminated
- Initiated
- 2014-06-27
- Posted
- 2014-09-11
- Terminated
- 2015-07-30
- 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
- Root cause
- Labeling False and Misleading
- Action
- Life Force of Tampa LLC sent an URGENT: MEDICAL DEVICE RECALL letter dated June 27, 2014 to all affected customers. The letter instructed the customers to: 1) Immediately remove and discard all copies of the labeling material. 2) Remove all electronic copies of the materials from any publicly accessible locations (e.g. website). 3) Complete and return the Acknowledgment form to Life Force of Tampa. For questions or concerns contact Douglas G. Cornell at (813) 961-4655.
- Quantity
- 10
- Distribution
- Nationwide Distribution in the states of AZ, FL, MD, NV, OK, PA, and TX.
- Lot, serial or model codes
- ALL Life Force Chambers
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LGM
- Firm FEI
- 3010406411
- Firm city
- Tampa
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28