EMD Millipore recalls Lugol's Iodine Solution 500ML (Lot 3124) due to improper seal causing iodine vapor loss over time. Affected customers should check product details and contact for remedy.
Due to the incorrect packaging utilized with lot 3124, there' s an improper seal between the cap and bottle. With an improper seal the Assay (current specification of 24.8 to 27.2 mL) is expected to continue to drop over time as iodine vapors continue to dissipate from the bottles.
EMD Millipore is recalling Lugol's Iodine Solution 500ML (Lot 3124) because the bottle's seal is faulty, leading to iodine vapor escaping over time. This could mean the solution becomes less effective as it's used for medical purposes.
The bottle's seal is incorrect, causing iodine vapors to escape gradually. This leads to the solution's concentration dropping below the required level (24.8 to 27.2 mL) over time, making it less effective for intended medical use.
People who own or use Lugol's Iodine Solution 500ML with Lot Number 3124 are affected. Those using the product for medical purposes may experience reduced effectiveness over time.
Check for the product name 'Lugol's Iodine Solution 500ML' and the lot number 3124 on the label. The product was sold by EMD Millipore Corporation.
Verify the product name and lot number 3124 on the label to confirm if it's affected.
The product has an improper seal that causes iodine vapors to escape over time, reducing the solution's effectiveness.
Check the product label for the lot number 3124. If affected, contact EMD Millipore for further instructions.
The hazard is low risk; the solution may become less effective over time but does not pose an immediate safety risk.
We’ve drafted a message you can send EMD Millipore to request your refund or repair — edit it as you like.
Subject: Recall Z-0408-2024 — EMD Millipore EMD Millipore Hello, I own a EMD Millipore that is covered by recall Z-0408-2024 from EMD Millipore. 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.
