MAIN PRODUCTS INC

FDA Regulatory Profile

MAIN PRODUCTS INC appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0626-2024, Class I) was initiated on July 18, 2024.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0626-2024Class IUmary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.July 18, 2024