Bel Brands USA

FDA Regulatory Profile

Bel Brands USA has 1 FDA recall, 16 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
F-0029-2018 · Class II · Oct 6, 2017
Latest inspection
Aug 27, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections16Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-0029-2018Class IIMerkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 76306-60200Oct 6, 2017

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 27, 2026Chicago, ILFood/CosmeticsNo Action Indicated (NAI)3010135671
Jul 10, 2025Brookings, SDFood/CosmeticsNo Action Indicated (NAI)3010784660
May 8, 2024Leitchfield, KYFood/CosmeticsNo Action Indicated (NAI)1021692
Jul 22, 2022Chicago, ILFood/CosmeticsNo Action Indicated (NAI)3010135671
May 25, 2021Brookings, SDFood/CosmeticsNo Action Indicated (NAI)3010784660
May 18, 2021Little Chute, WIFood/CosmeticsNo Action Indicated (NAI)2124123
Sep 12, 2019Leitchfield, KYFood/CosmeticsNo Action Indicated (NAI)1021692
Sep 13, 2018Chicago, ILFood/CosmeticsNo Action Indicated (NAI)3010135671
Dec 15, 2017Little Chute, WIFood/CosmeticsNo Action Indicated (NAI)2124123
Jun 20, 2017Hilbert, WIFood/CosmeticsNo Action Indicated (NAI)3009866132
Jun 7, 2017Brookings, SDFood/CosmeticsNo Action Indicated (NAI)3010784660
Dec 16, 2014Little Chute, WIFood/CosmeticsNo Action Indicated (NAI)2124123
Mar 22, 2013Leitchfield, KYFood/CosmeticsNo Action Indicated (NAI)1021692
Jan 9, 2013Little Chute, WIFood/CosmeticsNo Action Indicated (NAI)2124123
May 5, 2010Little Chute, WIFood/CosmeticsNo Action Indicated (NAI)2124123
Jul 14, 2009Little Chute, WIFood/CosmeticsNo Action Indicated (NAI)2124123

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 3010135671Chicago, IL3Aug 27, 2026
FEI 3010784660Brookings, SD3Jul 10, 2025
FEI 1021692Leitchfield, KY3May 8, 2024
FEI 2124123Little Chute, WI6May 18, 2021
FEI 3009866132Hilbert, WI1Jun 20, 2017

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