RECALL RECORD — CLASS IIRecall closedF-0340-2023/FDA enforcement

Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, Packaged Under the Following Brands…

What you need to know

Class II
  • What happened

    Raw material tested positive for Cronobacter sakazakii.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Cronobacter bacteria can cause severe illness, especially in infants and premature babies.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameOrtho Molecular Products INC
Recalling firmOrtho Molecular Products, INC.Stevens Point, WI, United States
UPC / barcodes
6 15033 00608 28 56420 00632 66 15033 04608 86 15033 01608 16 15033 60608 46 15033 61608 3
Lot / date codes
  • Lot 87121 Product Number 608445, 608445C, 608445CAN, and 608445U UPC 615033006082, 615033016081, 615033046088, and 615033606084 Expiration Date 06/30/23 Lot 87059 Product Number 608445, 608445C, 608445CAN, UTZ100-1300168, 608445U UPC 615033006082, 615033016081, 615033046088, 615033606084, and 856420006326 Expiration Date 06/30/23
Distribution area
Nationwide

Nationwide. Outside the US to Canada.

United States, Canada

Quantity affected4, 929 bottles
Recall initiationFDA report date: February 15, 2023
FDA recall numberF-0340-2023

Beyond the headline

The recall, in context

Ortho Molecular Products, INC. initiated this supplements recall on January 12, 2023. The FDA enforcement report states: Raw material tested positive for Cronobacter sakazakii. The FDA report lists distribution as: Nationwide. Outside the US to Canada.

The FDA enforcement report describes the reason as: Raw material tested positive for Cronobacter sakazakii.

Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, Packaged Under the Following Brands… was made or distributed by Ortho Molecular Products, INC. in Stevens Point, WI, United States. This page reflects FDA report F-0340-2023, dated February 15, 2023.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, cronobacter bacteria can cause severe illness, especially in infants and premature babies.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Cronobacter

Symptoms to watch for

In infants, possible poor feeding, irritability, temperature changes, jaundice, grunting or seizures. In adults, fever and gastrointestinal symptoms may occur.

When symptoms may appear

The timing varies; infant infections can become serious quickly.

Higher-risk groups

Infants, especially premature or low-birth-weight babies, and immunocompromised people are at highest risk.

What to do now

  1. 1Do not feed the affected product to an infant or anyone in a high-risk group.
  2. 2If an infant has poor feeding, unusual irritability, fever or breathing problems, seek urgent medical care.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and follow the recall notice for safe disposal.

Powdered infant formula and infant-feeding products warrant extra caution.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, Packaged Under the Following Brands… recall?

Ortho Molecular Products INC recalled Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, Packaged Under the Following Brands… in an FDA Class II enforcement action reported as F-0340-2023. Raw material tested positive for Cronobacter sakazakii.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Do not feed the affected product to an infant or anyone in a high-risk group. If an infant has poor feeding, unusual irritability, fever or breathing problems, seek urgent medical care. Keep the packaging, contact the retailer or manufacturer for a refund, and follow the recall notice for safe disposal.

Is the Ortho Molecular Products INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0340-2023. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.