Miralax powder for solution (30 doses) recalled due to storage outside label specifications. Consumers should check product details and contact manufacturer for guidance.
CGMP Deviations: products were stored outside the drug label specifications.
Miralax powder for solution (30 doses) is being recalled because it was stored outside the drug label specifications. This could lead to product contamination, though the risk is not severe enough to require immediate discontinuation.
The product was stored outside the drug label specifications, which could lead to contamination. This is a manufacturing issue related to storage conditions, not a direct safety hazard like a chemical reaction or physical damage.
People who purchased Miralax powder for solution (30 doses) from pharmacies or retailers. Those with specific medical conditions requiring precise medication timing may be at slightly higher risk.
Check for the product name 'Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ (510 g)' on the bottle. The NDC code 11523-7234-4 is also listed on the packaging.
Look for the product name and NDC code 11523-7234-4 on the bottle to confirm if it's recalled.
The recall is due to storage deviations, not a direct safety hazard. The product is safe to use if stored correctly, but the recall is for potential contamination risk.
Check for the product name 'Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ (510 g)' and NDC code 11523-7234-4 on the bottle.
The recall does not require immediate action. Check product details and contact the manufacturer for guidance if you have concerns.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1319-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1319-2022 from Mckesson Medical-Surgical. 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.
