CLASS III ONGOING Food recall · Reported 25 Mar 2026 · FDA Enforcement Report

Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recalled

Winder Laboratories is recalling Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx, distributed in 25 states. The recall was initiated on 27 Oct 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14

Quantity recalled422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: H-0569-2026
FDA event ID: 97884
Recalling firm: Winder Laboratories, Winder, GA
Brand: Multivitamin
Classification: Class III
Status: Ongoing
Recall initiated: 27 Oct 2025
FDA classified: 13 Mar 2026
Reported: 25 Mar 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Potency & Assay
Product category: Vitamins

Timeline

27 Oct 2025	Recall initiated by company
13 Mar 2026	Classified by FDA	+137 days
25 Mar 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

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

Where it was distributed

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.

Alabama Arizona California Florida Hawaii Iowa Illinois Indiana Massachusetts Michigan Missouri Mississippi North Carolina New Jersey New York Oregon Pennsylvania Puerto Rico Rhode Island Tennessee

Questions about this recall

Why was it recalled?

Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

Which lots are affected?

Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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