Food recall

Professional Botanicals, Inc. recall: Product Name

Professional Botanicals, Inc., of Ogden, UT, recalled Product Name and 2 other products. The FDA's reason: “Products contains Magnesium Salicylate.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 18, 2025, and the FDA first listed it in its Enforcement Report of November 19, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

See FDA's words below

Status

Terminated

Closed December 31, 2025

The recall

Company
Professional Botanicals, Inc. (Ogden, UT)
Reason, in FDA's words
“Products contains Magnesium Salicylate.”
Where it was sold
Distributed nationwide: AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, and WY.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97552

The 3 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0181-2026 Class II

    Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 90, Dose: 2 Capsules. Product Sku: PB248

    Codes: Lot #: 71527

    Quantity: 452 Bottles

  • H-0182-2026 Class II

    Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.

    Codes: Lot #: 280914

    Quantity: 430 Bottles

  • H-0183-2026 Class II

    Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207

    Codes: Lot #: 290301

    Quantity: 253 Bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of November 19, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.