The Rejuvenator Chamber manufactured by Baro-Therapies recall
The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and pains brought on by changes in…
Why was The Rejuvenator Chamber manufactured by Baro-Therapies recalled?
The firm is distributing the Rejuvenator device without an approved 510(k).
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All Lots, Series and Codes
- Product
- The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and pains brought on by changes in…
- Recalling firm
- Baro-Therapies, Inc
- Quantity
- 10
- Distribution
- US Nationwide Distribution in the states of FL, GA, MS, TN and CO.
- Recall date
- October 8, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)