Winder Laboratories Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recall — FDA H-0569-2026
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Overview of recall records associated with Winder Laboratories, LLC, including dates, categories and classifications where available.
Classification mix: Class III: 2.
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
This page summarizes recall records in which the official source identifies Winder Laboratories, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.