EarthLab Inc

FDA Regulatory Profile

EarthLab Inc 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 (F-1347-2022, Class II) was initiated on May 11, 2022.

Summary

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

Recent Recalls

NumberClassProductDate
F-1347-2022Class IIWise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (fMay 11, 2022
F-1346-2022Class IIWise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3 times perMay 11, 2022
F-1348-2022Class IIWise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. May 11, 2022