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Data / Product recalls / Winder Laboratories, LLC

Winder Laboratories, LLC: 1 recall in 2026 (FDA)

Winder Laboratories, LLC, Winder, GA, is named in 1 recall in 2026: all from the FDA. The latest, on March 25, 2026, covers Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2.... Hazard: Subpotent. Source: FDA H-0569-2026.

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Country
United States
Location
Winder, GA
Agencies
U.S. Food and Drug Administration
First recall
March 25, 2026
Latest recall
March 25, 2026

Recalls

Each recall is listed once, with the role this firm has in it. Roles: recalling firm (1).

DateAgencyProductHazardUnitsRemedySold atRoleSource
March 25, 2026FDAMultivitamin 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...Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottlesVoluntary recall, Class III, ongoingRecalling firmaccessdata.fda.gov

By agency

AgencyRecallsLatest
U.S. Food and Drug Administration1March 25, 2026

Categories

CategoryRecalls
Dietary supplements1

Where each agency publishes its recalls

Updated March 25, 2026. Read from U.S. Food and Drug Administration recall data. CC0 1.0 (openFDA). Recalls are as the agencies published them: the CPSC, FDA (food enforcement reports) and NHTSA. A firm is one firm only when its exact name and country match; the CPSC and FDA print no firm ID. Stores are listed only when the agency's sold-at text names them, and an agency often adds that more stores sold the product. Categories are grouped by SpecStream from the words in the agency's title and product text. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.