Richin Trading Inc

FDA Regulatory Profile

Richin Trading Inc has 4 FDA recalls (4 Class I), 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
F-1454-2023 · Class I · Jul 19, 2023
Latest inspection
Jun 6, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls4 (4 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-1454-2023Class ITim Heung Yuen Black Melon Seed 6 oz., 12 oz. Ingredients: Melon Seeds, Salt, Sugar & Anise Seed…Jul 19, 2023
F-1300-2023Class ISun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Item Number 12153; UPC 715685121536; Net…Jun 9, 2023
F-1301-2023Class ISun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; Item Number 12152; UPC 715685121529; Net…Jun 9, 2023
F-1299-2023Class ISun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan; Item Number 12151; UPC 715685121512…Jun 9, 2023

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 6, 2025Alhambra, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125519
Jul 18, 2023Alhambra, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125519
Mar 1, 2016Alhambra, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125519
Feb 8, 2013Alhambra, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125519
Jun 3, 2009Alhambra, CAFood/CosmeticsNo Action Indicated (NAI)1000125519

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1000125519Alhambra, CA5Jun 6, 2025

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.