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Winder Laboratories, LLC

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20241
20251
20261
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FDA Recall United States Ongoing 2026 recordClass III

Winder Laboratories, LLC

Product
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx…
Reason
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
Published
March 25, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall Ongoing Historical recordClass III

Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL, Rx Only, For Oral Use Only, Manufactured By: /winder Laboratories, LLC, Winder, GA 30680. NDC: 75826-131-01

by Winder Laboratories, LLC

Reason
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
Published
December 17, 2025
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Phenazopyridine HCl Tablets USP, 100 mg, 100-count bottles, Rx Only, Manufactured by: Winder Laboratories, LLC. 716 Patrick Industrial Lane, Winder, GA 30680, NDC 75826-114-10,

by Winder Laboratories, LLC

Reason
Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.
Published
June 19, 2024
Distribution
Nationwide

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Showing 1–3 of 3 results

This page lists recalls that name Winder Laboratories, LLC as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.