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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Nutra Calm, Total Comfort, and Tense-X Recalled for Magnesium Salicylate

Agency Publication Date: November 12, 2025
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Summary

Professional Botanicals, Inc. is recalling 1,135 bottles of Nutra Calm, Total Comfort, and Tense-X dietary supplements because they contain magnesium salicylate, an ingredient not declared on the label for its potential effects. The recall affects 452 bottles of Nutra Calm, 430 bottles of Total Comfort, and 253 bottles of Tense-X. Consumers should return these products to the place of purchase for a refund.

Risk

Magnesium salicylate is a nonsteroidal anti-inflammatory drug (NSAID) that may pose risks to individuals with aspirin sensitivities, kidney issues, or those taking certain medications. No incidents or injuries have been reported to date.

What You Should Do

  1. Check your supplement bottles for the following product names and lot numbers: Nutra Calm (Lot 71527), Total Comfort (Lot 280914), or Tense-X (Lot 290301).
  2. If you have any of these products, stop using them immediately.
  3. Return the product to the place of purchase for a refund, throw it away, or contact Professional Botanicals, Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Nutra Calm (90 Count)
Variants: Vegetable Capsule, 90 Count, Dose: 2 Capsules
Item Code:
PB248
Lot Numbers:
71527

Recall #: H-0181-2026; Quantity: 452 Bottles; Package: 175cc HDPE Bottle

Product: Total Comfort (60 Count)
Variants: Vegetable Capsule, 60 Count, Dose: 2 Capsules
Item Code:
PB173
Lot Numbers:
280914

Recall #: H-0182-2026; Quantity: 430 Bottles; Package: 175cc HDPE Bottle

Product: Tense-X (60 Count)
Variants: Vegetable Capsule, 60 Count, Dose: 2 Capsules
Item Code:
PB207
Lot Numbers:
290301

Recall #: H-0183-2026; Quantity: 253 Bottles; Package: 175cc HDPE Bottle

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97552
Status: Resolved
Manufacturer: Professional Botanicals, Inc.
Sold By: Nationwide retailers
Manufactured In: United States
Units Affected: 3 products (452 Bottles; 430 Bottles; 253 Bottles)
Distributed To: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, Wyoming

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.