EMD Millipore Corporation

FDA Regulatory Profile

EMD Millipore Corporation appears in FDA public data with 2 recalls, 0 510(k) clearances, 4 FDA inspections, and 1 compliance action on record. Its most recent recall (Z-1185-2024, Class II) was initiated on January 26, 2024.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
4
Compliance Actions
1

Recent Recalls

NumberClassProductDate
Z-1185-2024Class IISchiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.January 26, 2024
Z-0408-2024Class IILugol s Iodine Solution 500ML, Part Number 624-71October 17, 2023