Home › Device types › IAM
Solution, Lugol'S
FDA product code IAM · Class 1 · Pathology
2
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-17 | EMD Millipore Corporation | 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 specificat |
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