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.
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
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.
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.
Prescription patients who received this specific morphine sulfate oral solution product. Healthcare providers who dispensed the product are most at risk for errors.
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.
Check the NDC code 75826-131-01 and lot number 1312405 on the product label to confirm it matches the recalled item.
The recall is due to a mispack size mismatch, not a safety hazard. The product itself is safe but the labeling error could lead to dosing confusion.
Look for the NDC code 75826-131-01 and lot number 1312405 on the product label. This product was manufactured in Winder, GA and expires September 2027.
No action is required for safety, but you should verify the product details to ensure you have the correct version.
We’ve drafted a message you can send Winder to request your refund or repair — edit it as you like.
Subject: Recall D-0223-2026 — Winder Winder Hello, I own a Winder that is covered by recall D-0223-2026 from Winder. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
