Severity
Low
LowClass IIIOngoing
FDA Food recall · Reported March 25, 2026
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Winder Laboratories, LLC recalled Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 … - a low-severity action.
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 … was recalled by Winder Laboratories, LLC in March 25, 2026. Reason: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.. Check the official notice for the remedy. Verify recall #H-0569-2026 with the FDA Food before acting.
The recall
Winder Laboratories, LLC issued this low-severity FDA Food recall-Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D..
- Low
- severity level
- Class III
- classification
- March 25, 2026
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0569-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0569-2026) was formally reported on March 25, 2026, with the manufacturer initiating the action on October 27, 2025. It is classified under Low severity (Class III), with a current status of Ongoing. Winder Laboratories, LLC is listed as the recalling firm, operating out of Winder, GA. Federal records list the affected scope as 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles.
The documented reason for this recall is: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D. Distribution data in the federal record shows the product reached: Product was shipped to the following states: AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI & WV.. 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, 6 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.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
Related Recalls
6
6 from same agency
Product description
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680
Reason for recall
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Ongoing |
| Recall number | H-0569-2026 |
| Date reported | March 25, 2026 |
| Date initiated | October 27, 2025 |
| Recalling firm | Winder Laboratories, LLC |
| Firm location | Winder, GA |
| Affected scope | 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles |
| Distribution | Product was shipped to the following states: AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI & WV. |
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 (H-0569-2026) 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? ▼
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680. Recalled by Winder Laboratories, LLC. Units affected: 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles.
Why was this product recalled? ▼
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on March 25, 2026. Severity: Low. Recall number: H-0569-2026.
Where was the recalled product distributed? ▼
Distribution: Product was shipped to the following states: AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI & WV..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0569-2026) 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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
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 March 25, 2026. 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.