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Savor Brands LLC.

FDA Regulatory Profile

Savor Brands LLC. has 2 FDA recalls (2 Class I), 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Savor Brands LLC." and its spelling variant "Savor Brands".

Latest recall: F-0671-2021 · Class I · Jun 2, 2021
Latest inspection: May 4, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	2 (2 Class I)	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	4	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Savor Brands LLC.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	Recall records	Class I
2026	1	0	0
2025	1	0	0
2024	0	0	0
2023	0	0	0
2022	0	0	0
2021	1	2	2
2020	0	0	0
2019	0	0	0
2018	1	0	0
2017	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent recalls

2 recall records on Jun 2, 2021.

Number	Class	Product	Date
F-0671-2021	Class I	Brown Rice Quinoa Farro, Fully Cooked Net Wt. 24 lbs, Item # 617322	Jun 2, 2021
F-0672-2021	Class I	Farro, Fully Cooked Net Wt. 24 lbs, Item # 641901	Jun 2, 2021

Recent FDA inspections

4 inspections from Sep 28, 2018 to May 4, 2026.

Date	Site	Product	Classification	FEI
May 4, 2026	Chesterfield, MO	Food/Cosmetics	No Action Indicated (NAI)	3013137389
Dec 16, 2025	Chesterfield, MO	Food/Cosmetics	Voluntary Action Indicated (VAI)	3013137389
Apr 8, 2021	Chesterfield, MO	Food/Cosmetics	No Action Indicated (NAI)	3013137389
Sep 28, 2018	Chesterfield, MO	Food/Cosmetics	Voluntary Action Indicated (VAI)	3013137389

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3013137389	Chesterfield, MO	4	May 4, 2026

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