FDA recall, , Moderate risk
Functional Formularies Organic Whole Foods Meal Replacement Peptide Formulas
The liquid meal replacement formulas may contain less vitamin A than stated.
Summary by Recall Canary from the FDA notice
What happened
Nutricia North America of White Plains, New York, recalled functional formularies Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley and functional formularies Nourish Organic Whole Foods Meal Replacement Peptide Formula Berry Medley Complete Plant Based Nutrition because the products may be subpotent for Vitamin A.
The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A, giving test results that showed a higher concentration of vitamin A than is actually in the product. The recall began on May 26, 2026, and was added to the FDA's Enforcement Report on July 13, 2026. The products were shipped to many states, Washington DC, Canada, and Australia.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
2 products
Affected if its UPC is listed.
A UPC is the number printed under a barcode.
Functional Formularies Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley Net wt. 12 oz (341g) Case
- UPC
- 8 57858 00453 3
- 8 57858 00450 2
- Affected units
- 24 count case with BEST IF USED BY DATES up to and including March 15, 2028 12 count package BEST IF USED BY DATES up to and including October 7, 2027
Functional Formularies Nourish Organic Whole Foods Meal Replacement Peptide Formula Berry Medley Complete Plant Based Nutrition Net wt. 12 oz (341g) Case
- UPC
- 8 57858 00445 8
- 8 57858 00447 2
- Affected units
- 24 count case with BEST IF USED BY DATES up to and including April 14, 2028 12 count package BEST IF USED BY DATES up to and including February 19, 2028
Recall details
- Company began the recall
- Sold in
Product was shipped to the following states: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Washington District of Columbia, Delaware, Florida, Georgia, Hawaii, 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, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia. Product was also shipped to Canada & Australia.
- Company
- Nutricia North AmericaWhite Plains, New York
- Hazard
- Wrong drug strength
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99074
- Recall numbers
- H-1152-2026 to H-1153-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
