Reported Oct 8, 2014 · Terminated

The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and…

Baro-Therapies, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baro-Therapies, Inc · 80 S Geronimo St · Miramar Beach, FL · 32550-8035

Is this the product you have?

  • The Rejuvenator Chamber manufactured by Baro-Therapies, Inc
  • Product UsageIndicated for relief from general aches and pains brought on by changes in the weather
Lot codes and dates
  • All Lots, Series and Codes
Amount recalled
10

Where it was sold

Why it was recalled

The firm is distributing the Rejuvenator device without an approved 510(k).

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 6, 2015 · Data as of Sep 19, 5:28 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.