Lugol s Iodine Solution 500ML, Part Number 624-71
Reported: December 6, 2023 Initiated: October 17, 2023 #Z-0408-2024
Product Description
Lugol s Iodine Solution 500ML, Part Number 624-71
Reason for Recall
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.
Details
- Recalling Firm
- EMD Millipore Corporation
- Units Affected
- 5 units
- Distribution
- US States: CA, NJ, WV
- Location
- Burlington, MA
Frequently Asked Questions
What product was recalled? ▼
Lugol s Iodine Solution 500ML, Part Number 624-71. Recalled by EMD Millipore Corporation. Units affected: 5 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 6, 2023. Severity: Moderate. Recall number: Z-0408-2024.
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