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Lower risk Food recall · FDA · Published December 20, 2021

Professional Formulas Inositol Supplement Recalled for Undeclared Niacin

Professional Formulas recalls inositol dietary supplement with UPC 4065111562 due to undeclared niacin. Consumers should check labels for the specific product and contact the manufacturer for details.

🇺🇸 FDA recall #F-0322-2023FoodProfessional Formulas ›
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Recalling firmProfessional Complementary Health Formulas, LLC5550 Rosewood St · Lake Oswego, OR 97035-5371
✎ GovInfoNow plain-language explainer

What happened, in plain English

Professional Formulas is recalling inositol dietary supplements sold in white plastic bottles with UPC 4065111562 because they contain undeclared niacin. This could pose a health risk if consumed without knowing the niacin content. Read more at govinfonow.com/recall/13550-professional-formulas-inositol-supplement-recalled-for-undeclared-niacin.

Source Summary by GovInfoNow · govinfonow.com/recall/13550-professional-formulas-inositol-supplement-recalled-for-undeclared-niacin · Updated October 4, 2026 · FDA enforcement record: FDA #F-0322-2023

Cite this page

“Professional Formulas Inositol Supplement Recalled for Undeclared Niacin.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13550-professional-formulas-inositol-supplement-recalled-for-undeclared-niacin. Based on FDA recall #F-0322-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0322-2023%22&limit=1).

Why it’s dangerous

The supplement contains undeclared niacin, which is a vitamin that can cause health issues if consumed in excess. The product was labeled for professional use only, but consumers may have taken it without knowing the niacin content.

Who’s affected

People who own or use the inositol supplement with UPC 4065111562. Those with specific health conditions requiring precise niacin intake may be at higher risk.

How to tell if you have this one

Check for a white plastic bottle labeled with the UPC 4065111562 and the phrase 'Professional Formulas COMPLEMENTARY HEALTH Inositol DIETARY SUPPLEMENT 360 Capsules'.

  • Brand
    Professional Formulas
  • Product
    Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PROFESSIONAL FORMULAS
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.
Recall numberProduct, codes & lotsQuantity
F-0322-2023Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Inositol DIETARY SUPPLEMENT 360 Capsules***Supplement Facts Serving Size: One Capsule***Inositol 920 mg***Other Ingredients: Vegetarian capsule (hypromellose and water) and vegetable stearate Professional Formulas PO Box 2034, Lake Oswego, OR 97035 Recommended Dosage: As a nutritional supplement, take one capsule up to 3 times daily, or as directed by your healthcare professional***FOR PROFESSIONAL USE ONLY"; Lot 103252640 bottles
F-0323-2023Vitamin B Complex packaged in white plastic bottle labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Vitamin B Complex DIETARY SUPPLEMENT 60 Capsules***Supplement Facts Serving Size: One Capsule***Vitamin B1 (as thiamine Hcl) 80mg 6667% Vitamin B2 (as riboflavin) 80 mg 6154% Vitamin B3 (as niacinamide) 80 mg NE 500% Vitamin B6 (as pyridoxine HCl) 80 mg 4706% Folic acid 667 mcg DFE 167% Vitamin B12 (as cyanocobalamin) 80 mcg 3333% Biotin 300 mcg 1000% Vitamin B5 (as calcium pantothenate) 80 mg 1600% Choline (as bitartrate) 80 mg 15%***Professional Formulas PO Box 2034, Lake Oswego, OR 97035 Recommended Dosage: As a nutritional supplement, take one capsule, or as directed by your healthcare professional***FOR PROFESSIONAL USE ONLY"; Lot 1092715299 bottles
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 4065111562 on the white plastic bottle with the specific label text.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 6 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: named in the noticeWIMichigan: nationwideMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: named in the noticeORNevada: nationwideNVWyoming: named in the noticeWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: named in the noticePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: nationwideCAUtah: named in the noticeUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: nationwideNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: nationwideTXFlorida: nationwideFL

FDA distribution: “Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: New York, Oregon, Pennsylvania, Utah, Wisconsin, Wyoming.

Recall timeline

FDA terminated this recall 15 months after the firm started it.

1. Firm started the recall: Dec 20, 202112. FDA classified it Class II: Jan 30, 202323. Published in FDA’s Enforcement Report: Feb 8, 202334. FDA terminated the recall: Apr 3, 2023420212023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0322-2023 (December 20, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0322-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA