# FDA recall Z-0408-2024

> **EMD Millipore Corporation** · Class II · device recall initiated 2023-10-17.

## Product

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.

## Distribution

US States: CA, NJ, WV

## Key facts

- **Recall number:** Z-0408-2024
- **Recalling firm:** EMD Millipore Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-17
- **Report date:** 2023-12-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Burlington, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0408-2024

## Citation

> AI Analytics. FDA recall Z-0408-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0408-2024. Source: US FDA. Licensed CC0.

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