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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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Low RiskFDA Food
Food & Beverages/Dietary Supplements

Calci-Max Dietary Supplement Recalled for Missing Zinc Content

Agency Publication Date: April 29, 2020
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Summary

Alfa Vitamins Laboratories, Inc. is recalling 1,877 bottles of Calci-Max Dietary Supplement because testing by the FDA found the product contained 0.0% of the zinc content promised on the label. This voluntary recall affects 60-capsule bottles from a specific production lot distributed domestically. Consumers who purchased this supplement should return it to the store where it was bought for a full refund or dispose of it immediately.

Risk

The product does not provide the nutritional benefits claimed on the label because it completely lacks zinc, which may result in consumers not receiving the intended dietary support.

What You Should Do

  1. Check your bottle for CALCI-MAX Dietary Supplement (60 capsules) with Lot number 31453, a manufacturing date (MFG) of 06 2019, and an expiration date (EXP) of 06 2022.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact Alfa Vitamins Laboratories, Inc. for further instructions.
  3. 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: CALCI-MAX Dietary Supplement (60 capsules)
Lot Numbers:
31453 (Exp 06 2022)
Date Ranges: Manufactured 06 2019

Manufactured for: DOMEL; Recall #: F-0926-2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85317
Status: Resolved
Manufacturer: Alfa Vitamins Laboratories, Inc.
Manufactured In: United States
Units Affected: 1877 bottles
Distributed To: Nationwide

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.