Dr. Berg Nutritionals, Liquid Vitamin D with Zinc Dietary Supplement ( Liquid Vitamin D ), Individual 1 FL OZ bottle (wi
Summary
The FDA issued a Class II for Dr. Berg Nutritionals, Liquid Vitamin D with Zinc Dietary Supplement ( Liquid Vi by Health & Wellness Center, Inc.. Reason: Product recalled because of the presence of mold and/or yeast found in amounts that exceed the product's established specifications ..
Details
Source
Food Recall
External ID
F-0092-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
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.
Lot/Code Info: Lot #2104637A, best by April 2023
Quantity Affected: 5,026 units
Reason for Recall
Product recalled because of the presence of mold and/or yeast found in amounts that exceed the product's established specifications .
Distribution
The product was distributed thru out the United States , via internet sales etc.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-09-24
Company
Alexandria, VA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Health & Wellness Center, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Health & Wellness Center, Inc. have FDA actions?
This is the only FDA action we have on record for Health & Wellness Center, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0092-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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