EUREKA INC
FDA Regulatory Profile
EUREKA INC has 1 FDA recall, 1 inspection, 1 510(k) clearance and 0 compliance actions on record.
What these totals cover: FDA records filed under the name "EUREKA INC" and its spelling variant "Eureka".
On this page: Recalls (1) · Inspections (1) · Facilities (1) · 510(k) clearances (1)
Latest recall H-0388-2026 · Class II · Sep 9, 2025Latest inspection May 7, 2025 · VAI
Latest 510(k) Nov 3, 1988
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Summary
Record counts and when each FDA source was last refreshed
Records Count Last refreshed Source as of Status
Recalls 1 Nov 8, 2026 File dated Nov 3, 2026 Current 510(k) clearances 1 Nov 8, 2026 File dated Nov 2, 2026 Current Inspections 1 Nov 13, 2026 Newest record Nov 5, 2026 Current Compliance actions 0 Nov 2, 2026 Newest record Oct 29, 2026 Current
1 recall record on Sep 9, 2025.
Number Class Product Date
H-0388-2026 Class II Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139 Sep 9, 2025
1 inspection on May 7, 2025.
Date Site Product Classification FEI
May 7, 2025 Pomona, CA Food/Cosmetics Voluntary Action Indicated (VAI) 3028783168
NAI No objectionable conditions or practices were found during the inspection.
VAI Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI Regulatory and/or administrative actions are recommended.
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1 inspected site, newest inspection first.
Facility Location Inspections Latest
FEI 3028783168 Pomona, CA 1 May 7, 2025
1 510(k) clearance on Nov 3, 1988.
K-Number Device Date
K882547 VARITEST Nov 3, 1988
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