EMD Millipore Corporation: Medical Device Recall in 2023 - (Recall #: Z-0408-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Lugol s Iodine Solution 500ML, Part Number 624-71

Product Classification:

Class II

Date Initiated: October 17, 2023

Date Posted: December 6, 2023

Recall Number: Z-0408-2024

Event ID: 93318

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.

Status: Ongoing

Product Quantity: 5 units

Code Information:

Lot Number 3124

Distribution Pattern:

US States: CA, NJ, WV

Voluntary or Mandated:

Voluntary: Firm initiated