Recall Register

Food, drugs, devices › Firms

Winder Laboratories, LLC

FDA recalling firm · 3 enforcement events · 3 product records · 2024–2025 · GA

Winder Laboratories, LLC has 3 FDA enforcement events on this register (3 product records) between 2024 and 2025: 2 drug and 1 food; the busiest year was 2025 with 2.

0% of its events are Class I; the most common class is Class III (2). 2 events are listed as ongoing; the recalling firm's address is in GA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
26 Nov 2025Morphine 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: 75826-131-01DrugClass III1Ongoing
27 Oct 2025Multivitamin 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 30680FoodClass III1Ongoing
28 May 2024Phenazopyridine 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,DrugClass II1Completed

By type and class

Drug2
Food1
Class III2
Class II1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

24
25
26
Enforcement events for Winder Laboratories, LLC by year initiated.

Questions and answers

How many FDA recalls has Winder Laboratories, LLC had?

3 enforcement events (3 product records) on this register, 2024–2025: 2 drug, 1 food.

Are any Winder Laboratories, LLC recalls ongoing?

2 events are listed as ongoing in the current openFDA export.

What class are Winder Laboratories, LLC recalls?

2 Class III, 1 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.