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RECALL RECORD — CLASS IIRecall closedF-0323-2023/FDA enforcement
Professional Complementary Health Formulas, LLC·Dietary Supplements·Dec 20, 2021

Vitamin B Complex Packaged in White Plastic Bottle Labeled in Part, "***Professional Formulas…

What you need to know

Class II

  • What happened

    Product recalled due to undeclared niacin.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • 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 nameProfessional Complementary Health Formulas, LLC
Recalling firmProfessional Complementary Health Formulas, LLCLake Oswego, OR, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot 1092715
Distribution area
Nationwide

Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.

United States

Quantity affected299 bottles
Recall initiationFDA report date: February 8, 2023
FDA recall numberF-0323-2023

Beyond the headline

The recall, in context

Professional Complementary Health Formulas, LLC initiated this supplements recall on December 20, 2021. The FDA enforcement report states: Product recalled due to undeclared niacin. The FDA report lists distribution as: Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.

The FDA enforcement report describes the reason as: Product recalled due to undeclared niacin.

Vitamin B Complex Packaged in White Plastic Bottle Labeled in Part, "***Professional Formulas… was made or distributed by Professional Complementary Health Formulas, LLC in Lake Oswego, OR, United States. This page reflects FDA report F-0323-2023, dated February 8, 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, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

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 lot and date codes 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

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

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 Vitamin B Complex Packaged in White Plastic Bottle Labeled in Part, "***Professional Formulas… recall?

Professional Complementary Health Formulas, LLC recalled Vitamin B Complex Packaged in White Plastic Bottle Labeled in Part, "***Professional Formulas… in an FDA Class II enforcement action reported as F-0323-2023. Product recalled due to undeclared niacin.

What are the symptoms of Undeclared allergen exposure?

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

How quickly can Undeclared allergen symptoms appear?

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Who is most at risk from Undeclared allergen?

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

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 eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

How do I get a refund from Professional Complementary Health Formulas, LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0323-2023 and keep the packaging, lot code and proof of purchase if you have them.

Is the Professional Complementary Health Formulas, LLC 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-0323-2023. 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

More recalls by Professional Complementary Health Formulas, LLC

View brand
Class II·

Professional Complementary Health Formulas, LLC

Inositol Packaged in White Plastic Bottle with

Product recalled due to undeclared niacin.

Nationwide (US)Supplements
Class II·

Professional Complementary Health Formulas, LLC

Professional Formulas Sublinqual B12 High-potency Dietary Supplement, 60-count Dissolvable…

Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.

IN, AZ, CA +31 more +2 countriesSupplements

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