FDA recall record
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 o...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of June 14, 2023. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Reason
Product recalled because of the presence of mold and/or yeast found in amounts that exceed the product's established specifications .
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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.
Code information listed by FDA
Lot #2104637A, best by April 2023
Distribution and firm information
Recalling firm listed by FDA: Health & Wellness Center, Inc.
Firm location listed by FDA: Alexandria, VA, United States
Distribution reported by FDA: The product was distributed thru out the United States , via internet sales etc.
Product quantity listed by FDA: 5,026 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.