Sunset Natural Products Inc.

FDA Regulatory Profile

Sunset Natural Products Inc. appears in FDA public data with 173 recalls, 0 510(k) clearances, 4 FDA inspections, and 2 compliance actions on record. Its most recent recall (F-1026-2017, Class II) was initiated on October 13, 2015.

Summary

Total Recalls
173
510(k) Clearances
0
Inspections
4
Compliance Actions
2

Recent Recalls

NumberClassProductDate
F-1026-2017Class IIProstamax Dietary Supplement (unknown container size)October 13, 2015
F-1067-2017Class IIVia Sex Dietary Supplement (unknown container size)October 13, 2015
F-1080-2017Class IIGlow Dietary Supplement (unknown container size)October 13, 2015
F-0989-2017Class IIBees, bulk capsulesOctober 13, 2015
F-0939-2017Class IIMagnun Plus, (30 per bottle)October 13, 2015
F-0958-2017Class IIChardon De Marie, 60 capsules per bottleOctober 13, 2015
F-1015-2017Class IISugar Burner Dietary Supplement (unknown container size)October 13, 2015
F-0975-2017Class IIBima, bulk capsulesOctober 13, 2015
F-0957-2017Class IITyrosine Formula, 90 capsules per bottleOctober 13, 2015
F-1053-2017Class IIPahaya Dietary Supplement (unknown container size)October 13, 2015
F-0993-2017Class IIAbte, bulk capsulesOctober 13, 2015
F-0920-2017Class IICrea Care, (100,000 capsule bulk)October 13, 2015
F-1032-2017Class IIProga Dietary Supplement (unknown container size)October 13, 2015
F-1041-2017Class IIMarx Dietary Supplement (unknown container size)October 13, 2015
F-1046-2017Class IIGoji Dietary Supplement (unknown container size)October 13, 2015
F-0996-2017Class IIResin, bulk capsulesOctober 13, 2015
F-0953-2017Class IIABS Reducer, 60 capsules per bottleOctober 13, 2015
F-1000-2017Class IIPritos, bulk capsulesOctober 13, 2015
F-0981-2017Class IIMemory, bulk capsulesOctober 13, 2015
F-1049-2017Class IIEchinacea Dietary Supplement (unknown container size)October 13, 2015