Winder Morphine Sulfate Oral Solution Recall: Mispack Size Mismatch
Winder Laboratories recalls Morphine Sulfate Oral Solution 100mg/5mL (20mg/mL) 30mL due to mispack size mismatch between label and bottle. This is a prescription-only product.
Lower-risk recall
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
Contact the company
What happened, in plain English
Winder Laboratories is recalling a specific morphine sulfate oral solution product because the bottle size in the carton doesn't match what's labeled. This mismatch could lead to incorrect dosing if the product is used without proper verification. Read more at govinfonow.com/recall/31626-winder-morphine-sulfate-oral-solution-recall-mispack-size-mismatch.
Source Summary by GovInfoNow · govinfonow.com/recall/31626-winder-morphine-sulfate-oral-solution-recall-mispack-size-mismatch · Updated August 17, 2026 · FDA enforcement record: FDA #D-0223-2026
Cite this page
“Winder Morphine Sulfate Oral Solution Recall: Mispack Size Mismatch.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31626-winder-morphine-sulfate-oral-solution-recall-mispack-size-mismatch. Based on FDA recall #D-0223-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0223-2026%22&limit=1).
Why it’s dangerous
The carton label states a different bottle size than what's actually in the package. This mismatch could cause confusion about the correct dosage amount if the product is used without verifying the actual bottle size.
Who’s affected
Prescription patients who received this specific morphine sulfate oral solution product. Healthcare providers who dispensed the product are most at risk for errors.
How to tell if you have this one
Check for the product name 'Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL' with NDC 75826-131-01 and lot number 1312405. This product was manufactured in Winder, GA and expires September 2027.
- Brand
Winder- Category
Drug
What to do — step by step
Verify Product Details
Check the NDC code 75826-131-01 and lot number 1312405 on the product label to confirm it matches the recalled item.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 21 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using this product?
No action is required for safety, but you should verify the product details to ensure you have the correct version.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0223-2026 (November 26, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0223-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.