Hyobin LLC

FDA Regulatory Profile

Hyobin LLC appears in FDA public data with 3 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0383-2021, Class II) was initiated on April 6, 2021.

Summary

Total Recalls
3
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0383-2021Class IITriple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, DistrApril 6, 2021
D-0381-2021Class IIPremierZen Extreme 3000, packaged in cardboard blisters containing one capsule per card, DistributApril 6, 2021
D-0382-2021Class IIPremierZen Black 5000, packaged in cardboard blisters containing one capsule per card, DistributedApril 6, 2021