
Functional Formularies: 2 products
Nutricia recalls Liquid Hope and Nourish organic meal replacement formulas due to subpotent Vitamin A.
Stop using the recalled products and contact Nutricia North America for a refund or replacement. Do not consume the product if you rely on it for complete nutrition, and consult your healthcare provider if you have concerns about vitamin A intake.
Why it was recalled
Nutricia North America is recalling Liquid Hope and Nourish Organic Whole Foods Meal Replacement Peptide Formulas because they are subpotent for Vitamin A. The testing laboratory used the wrong method, resulting in higher reported vitamin A levels than actually present. Consumers with these products should contact Nutricia North America for a refund or replacement.
Is mine affected?
Check the lot code and best-by (or expiration) date printed on your package. Yours is affected if it matches one below.
| Product | NDC / UPC | Recall # |
|---|---|---|
| functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ… | UPC 8 57858 00453 3, UPC 8 57858 00450 2 | H-1152-2026 |
| functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY COMPLETE PLANT BASED… | UPC 8 57858 00445 8, UPC 8 57858 00447 2 | H-1153-2026 |
Where it was sold
Distributed in Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, 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, and West Virginia.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification
