CLASS II Device recall · Reported 17 Sep 2014 · FDA Enforcement Report

Life Force Chamber recalled

Life Force of Tampa is recalling Life Force Chamber, distributed nationwide in the US. The recall was initiated on 27 Jun 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesALL Life Force Chambers
Quantity recalled10

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2625-2014
FDA event ID
69043
Recalling firm
Life Force of Tampa, Tampa, FL
Classification
Class II
Status
Terminated
Recall initiated
27 Jun 2014
FDA classified
11 Sep 2014
Reported
17 Sep 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Device Malfunction

Timeline

27 Jun 2014Recall initiated by company
11 Sep 2014Classified by FDA+76 days
17 Sep 2014Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.

Where it was distributed

Nationwide Distribution in the states of AZ, FL, MD, NV, OK, PA, and TX.

Nationwide ArizonaFloridaMarylandNevadaOklahomaPennsylvaniaTexas

Questions about this recall

Is Life Force Chamber recalled?

Yes. Life Force of Tampa recalled Life Force Chamber on 27 Jun 2014. The recall is Class II and its status is Terminated. Recall number Z-2625-2014.

Why was it recalled?

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

Which lots are affected?

ALL Life Force Chambers

Where was it sold?

Nationwide Distribution in the states of AZ, FL, MD, NV, OK, PA, and TX.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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