Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported February 8, 2023
Inositol 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
Product recalled due to undeclared niacin.
Professional Complementary Health Formulas, LLC recalled Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PR… - a moderate-severity action.
Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PR… was recalled by Professional Complementary Health Formulas, LLC in February 8, 2023. Reason: Product recalled due to undeclared niacin.. Check the official notice for the remedy. Verify recall #F-0322-2023 with the FDA Food before acting.
The recall
Professional Complementary Health Formulas, LLC issued this moderate-severity FDA Food recall-Product recalled due to undeclared niacin..
- Moderate
- severity level
- Class II
- classification
- February 8, 2023
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0322-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0322-2023) was formally reported on February 8, 2023, with the manufacturer initiating the action on December 20, 2021. It is classified under Moderate severity (Class II), with a current status of Terminated. Professional Complementary Health Formulas, LLC is listed as the recalling firm, operating out of Lake Oswego, OR. Federal records list the affected scope as 40 bottles.
The documented reason for this recall is: Product recalled due to undeclared niacin. Distribution data in the federal record shows the product reached: Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
40 bottles
Related Recalls
6
2 from same agency
Product description
Inositol 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"
Reason for recall
Product recalled due to undeclared niacin.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0322-2023 |
| Date reported | February 8, 2023 |
| Date initiated | December 20, 2021 |
| Recalling firm | Professional Complementary Health Formulas, LLC |
| Firm location | Lake Oswego, OR |
| Affected scope | 40 bottles |
| Distribution | Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0322-2023) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Inositol 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". Recalled by Professional Complementary Health Formulas, LLC. Units affected: 40 bottles.
Why was this product recalled? ▼
Product recalled due to undeclared niacin.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on February 8, 2023. Severity: Moderate. Recall number: F-0322-2023.
Where was the recalled product distributed? ▼
Distribution: Inositol was distributed in NY, OR, PA, UT, WI, and WY. Vitamin B Complex was distributed nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0322-2023) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported February 8, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.