← FDA ENFORCEMENT
D-0224-2024Class I

Botanical Be

Recalling firm
Botanical Be
Product type
Drug
Status
Ongoing
Report date
2023-12-06
Distribution
USA Nationwide
Firm state
TX
Product quantity
235 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

Product description

Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol Ocampo # 65 Local D, Delegacion Xochimilco CP 16800, Mexico DF, UPC 7 501031 111138

Code / lot info

Lot 35421, exp 12/19/2025

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.