El Chilar HF

FDA Regulatory Profile

El Chilar HF has 6 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
F-1743-2024 · Class II · Jul 29, 2024
Latest inspection
Sep 8, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls6Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-1743-2024Class IIEl Chilar, Canela Molida, Ground Cinnamon NET WT. 1.25 Oz (35g) , Spices Herbs, BOPP Bag, 12 units…Jul 29, 2024
F-1092-2024Class IIEl Chilar, Canela Molida, Ground Cinnamon NET WT. 1.25 Oz (35g) , BOPP Bag, 12 units per casesMar 4, 2024
F-0410-2024Class IIIORALE! CAMARON MOLIDO, GROUND SHRIMP, NET WT. 2 OZ. 57 g (in paper cartons) (12 packages per case of…Sep 20, 2023
F-0413-2024Class IIIBLUM'S SHRIMP SHRED DRIED SHRIMP, COOKED IN SALT WATER, BLUM'S SEAFOOD PRODUCTS LLC, Net Wt. 50 LBS…Sep 20, 2023
F-0411-2024Class IIIORALE! CAMARON NATURAL, NATURAL SHRIMP, NET WT. 2 OZ. 57 g (in paper cartons) (12 packages per case…Sep 20, 2023
F-0412-2024Class IIIEL CHILAR CAMARON NATURAL, NATURAL SHRIMP, NET WT. 2 Oz. (57g) (in paper cartons) (12 packages per…Sep 20, 2023

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 8, 2025Apopka, FLFood/CosmeticsVoluntary Action Indicated (VAI)3004263103
Sep 18, 2023Apopka, FLFood/CosmeticsVoluntary Action Indicated (VAI)3004263103
Mar 21, 2013Apopka, FLFood/CosmeticsVoluntary Action Indicated (VAI)3004263103
Mar 7, 2011Apopka, FLFood/CosmeticsVoluntary Action Indicated (VAI)3004263103
Sep 17, 2010Apopka, FLFood/CosmeticsNo Action Indicated (NAI)3004263103
Dec 19, 2008Apopka, FLFood/CosmeticsNo Action Indicated (NAI)3004263103

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 3004263103Apopka, FL6Sep 8, 2025

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