Winder Laboratories recalls
Winder Laboratories appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2026-03-25.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 3 |
|---|---|
| Published | 2024-06-19 to 2026-03-25 |
| By agency | FDA Drug (2), FDA Food (1) |
| By classification | Class III (2), Class II (1) |
| By status | ongoing (2), completed (1) |
| Distribution named in notices | AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, US, UT, WA, WI, WV |
Recalls
- Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2
FDA Food · Class III · 2026-03-25 · Winder Laboratories
Reason: Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D. - Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL, Rx Only, For Oral Use Only, Manufactured By: /winder Laboratories, LLC,…
FDA Drug · Class III · 2025-12-17 · Winder Laboratories
Reason: Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton. - Phenazopyridine HCl Tablets USP, 100 mg, 100-count bottles, Rx Only, Manufactured by: Winder Laboratories, LLC. 716 Patrick Industrial Lane…
FDA Drug · Class II · 2024-06-19 · Winder Laboratories
Reason: Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained Phenobarbital tablets 16.2 mg.