Multivitamin Recall: Winder Fluoride Chewable Tablets
Announced 2025-12-17 · FDA
The recall concerns Winder Laboratories' multivitamin with fluoride chewable tablets (grape flavor) due to subpotent Vitamin D. The issue was found during an FDA inspection and is listed as low severity. Affected lots are Lot 1692303 (SN: 138909557498, EXP: 2025-10-26), Lot 1692304 (SN: 131163901709, EXP: 2025-10-26), and Lot 1712301 (SN: 163590222021, EXP: 2025-11-14); products were distributed to multiple states including 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.
| Brand | Winder Laboratories, LLC |
|---|---|
| Product | 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 | Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D. |
| Severity | low |
| Units affected | 3528 |
| 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. |
| Agency | FDA |
| Recall / campaign no. | Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14 |
WHAT YOU SHOULD DO
- If you have any recalled lots, stop using them immediately.
- Check your bottle for Lot numbers 1692303, 1692304, or 1712301 and corresponding expiration dates; discard or return the product to the place of purchase.
- Consult your healthcare provider or pharmacist for guidance on alternatives.
- If you experience adverse effects, seek medical care and report them.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.