Recall Radar

Health & Wellness Center recalls Dr. Berg Nutritionals: contamination

November 10, 2021 · Health & Wellness Center Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallProduct recalled because of the presence of mold and/or yeast found in amounts that exceed the product's established specifications .

Find the official FDA enforcement report

Recall at a glance

Recalling company
Health & Wellness Center
Location
Alexandria, VA
Reported by FDA
November 10, 2021
Recall started
September 24, 2021
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Other contamination

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Dr. Berg Nutritionals, Liquid Vitamin D with Zinc Dietary Supplement ( Liquid Vitamin D ), Individual 1 FL OZ bottle (with no secondary packaging), Glass bottle. The label of the Liquid Vitamin D product includes the following storage instructions: Store in a cool, dark place, with a lid.
    Quantity: 5,026 units
    Codes: Lot #2104637A, best by April 2023

Where it was distributed

The product was distributed thru out the United States , via internet sales etc.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Health & Wellness Center recalled 1 product, including Dr. Berg Nutritionals, Liquid Vitamin D with Zinc Dietary Supplement ( Liquid Vitamin D ), Individual 1 FL OZ bottle (with no secondary….

Why was it recalled?

Product recalled because of the presence of mold and/or yeast found in amounts that exceed the product's established specifications .

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

The product was distributed thru out the United States , via internet sales etc.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in supplements and infant formula

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.