DrugDec 6, 2023
Botanical Be Artri King Reforzado con Origa y Omega 3 tablets recall — FDA D-0224-2024
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Class IFDA: OngoingBotanical Be
Recall history in this database
Classification mix: Class I: 2.
DrugDec 6, 2023
Botanical Be Reumo Flex caplets recall — FDA D-0225-2024
Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.
Class IFDA: OngoingBotanical Be
Understanding this recall history
This page summarizes recall records in which the official source identifies Botanical Be 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.