Yamtun7

FDA Regulatory Profile

Yamtun7 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-0654-2021, Class I) was initiated on May 11, 2021.

Summary

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

Recent Recalls

NumberClassProductDate
D-0654-2021Class IPoseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA,May 11, 2021