Home / Recalls / Medical Devices
EMD Millipore Corporation recalls Lugol s Iodine Solution 500ML, Part Number 624-71
Recalled December 6, 2023 · FDA recall Z-0408-2024 · EMD Millipore
Hazard
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. · FDA Class II
Units
5 units
Sold at
US States: CA, NJ, WV
Description
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.
Product
Lugol s Iodine Solution 500ML, Part Number 624-71
Manufacturer(s)
EMD Millipore Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →