Nutricia North America Recall: Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

🇺🇸 United States

1. May 26, 2026 - Recall initiated
2. July 22, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-1153-2026

Event ID

99074

Status

Ongoing

Classification

Class II

Company

Nutricia North America

Product description

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, package UPC 8 57858 00447 2

Quantity

2,050cs/12/12oz pouches + 55,310cs/24/12oz pouches

Reason

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

Recall initiation date

May 26, 2026

Report date

July 22, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Product was shipped to the following states: 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. Product was also shipped to Canada & Australia.

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 27, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 99074 with 1 other product entry in Public Health Trace.

Responsible company: Nutricia North America

Other recalls from Nutricia North America

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alaska	1
Alabama	1
Arkansas	1
Arizona	1
California	1
Colorado	1
Connecticut	1
District of Columbia	1
Delaware	1
Florida	1
Georgia	1
Hawaii	1
Iowa	1
Idaho	1
Illinois	1
Indiana	1
Kansas	1
Kentucky	1
Louisiana	1
Massachusetts	1
Maryland	1
Maine	1
Michigan	1
Minnesota	1
Missouri	1
Mississippi	1
Montana	1
North Carolina	1
North Dakota	1
Nebraska	1
New Hampshire	1
New Jersey	1
New Mexico	1
Nevada	1
Ohio	1
Oklahoma	1
Oregon	1
Pennsylvania	1
Rhode Island	1
South Carolina	1
South Dakota	1
Tennessee	1
Texas	1
Utah	1
Virginia	1
Vermont	1
Washington	1
Wisconsin	1
West Virginia	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 27, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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