Nutricia North America Recalls Liquid Hope Organic Meal Replacement
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Nutricia North America is recalling functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY due to subpotency for Vitamin A.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 9, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, food.
What Happened
Nutricia North America is conducting a voluntary recall of functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY because the product is subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A, resulting in higher reported concentrations than what is actually in the product.
Which Products Are Affected
The recall involves functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g), with case UPC 8 57858 00453 3 and package UPC 8 57858 00450 2. Affected quantities include 1,363 cases of 12/12oz pouches and 16,298 cases of 24/12oz pouches. The 24-count cases have BEST IF USED BY DATES up to and including March 15, 2028, and the 12-count packages have BEST IF USED BY DATES up to and including October 7, 2027. The product was shipped to AK, AL, AR, AZ, CA, CO, CT, Washington DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, as well as Canada and Australia. This is FDA recall number H-1152-2026, a Class II recall.
What You Should Do
Consumers should verify the BEST IF USED BY dates on 24-count cases and 12-count packages against the affected ranges and contact Nutricia North America for further guidance on the recalled product.
Why This Matters
This ongoing Class II recall affects a widely distributed organic meal replacement product across the United States, Canada, and Australia.
Source
FDA Enforcement Report, recall number H-1152-2026, report date 20260722.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,702 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.