Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lugol s Iodine Solution 500ML Recalled by EMD Millipore Corporation Due to Due to the incorrect packaging utilized with lot...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact EMD Millipore Corporation directly.
Affected Products
Lugol s Iodine Solution 500ML, Part Number 624-71
Quantity: 5 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 3 states: CA, NJ, WV
About EMD Millipore Corporation
EMD Millipore Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report