FDA recall record

Baro-Therapies The Rejuvenator Chamber manufactured by Baro-Therapies, Inc recall — FDA Z-2734-2014

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

Class IIclassification
Z-2734-2014official record ID
Oct 8, 2014report date

Recall record at a glance

Official recordZ-2734-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaro-Therapies, Inc.
Report dateOct 8, 2014
Recall initiation dateAug 8, 2014
Quantity10
LocationMiramar Beach, FL, United States

Official product description

The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and pains brought on by changes in the weather.

Why the product was recalled

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

Distribution information

US Nationwide Distribution in the states of FL, GA, MS, TN and CO.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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