FDA recalls · H-0569-2026
Winder Laboratories, LLC recall
- FoodMultivitamin 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
- ReasonSubpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- ClassClass III: the food is unlikely to cause health problems
- StatusOngoing
- DatesFirm started it 2025-10-27. In FDA's enforcement report 2026-03-25.
- Sold inProduct 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.
- Amount422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles
- CodesLot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14
- FirmWinder Laboratories, LLC, Winder, GA · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, H-0569-2026. Class meanings: FDA.