Overview of recall records associated with RoyalVibe Health Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established. There is a possibility of customers'…
This page summarizes recall records in which the official source identifies RoyalVibe Health Ltd. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
