epa_echo
1 records
fda
2 records
FDA Recall: LED Technologies, LLC — Class II
20160504
Incorrect Power Supply in the package, rendering the device inoperable. | Product: reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Ligh
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FDA Device Recall: reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usa
2016-05-04
Class II — Incorrect Power Supply in the package, rendering the device inoperable.
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