Monfitello

FDA Regulatory Profile

Monfitello has 2 FDA recalls (2 Class I), 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
F-2372-2017 · Class I · May 26, 2017
Latest inspection
Dec 17, 2019 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls2 (2 Class I)Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-2372-2017Class IPRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0…May 26, 2017
F-2373-2017Class IPrivate Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET WT 4 OZ (113g)…May 26, 2017

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 17, 2019Lachine, CanadaFood/CosmeticsOfficial Action Indicated (OAI)3007992770

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 3007992770Lachine, Canada1Dec 17, 2019

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