FDA recall record

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 Iclassification
D-0224-2024official record ID
Dec 6, 2023report date

Recall record at a glance

Official recordD-0224-2024
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmBotanical Be
Report dateDec 6, 2023
Recall initiation dateOct 20, 2023
Quantity235 bottles
LocationEl Paso, TX, United States

Official 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

Why the product was recalled

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

Distribution information

USA Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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