Recall record at a glance
| Official record | H-0569-2026 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Ongoing |
| Recalling firm | Winder Laboratories, LLC |
| Report date | Mar 25, 2026 |
| Recall initiation date | Oct 27, 2025 |
| Quantity | 422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles |
| Location | Winder, GA, United States |
Official 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
Why the product was recalled
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Distribution information
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 to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
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