Global Garlic, Inc.

FDA Regulatory Profile

Global Garlic, Inc. has 3 FDA recalls (2 Class I), 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Global Garlic, Inc." and its spelling variant "Global Garlic".

Latest recall
F-2409-2017 · Class I · May 11, 2017
Latest inspection
May 11, 2023 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls3 (2 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

Global Garlic, Inc.: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202200000
202100000
202000000
201900000
201800000
201700022

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

3 recall records from Mar 8, 2016 to May 11, 2017.

NumberClassProductDate
F-2409-2017Class IDe Mi Pais, Queso Fresco, Whole Milk Cheese, Net Wt 16 oz.. (1 lb)May 11, 2017
F-2410-2017Class IQueso Fresco x LB (Barra)/ Whole Milk Cheese, Net Wt 5-6 lbs.May 11, 2017
F-2600-2016Class IIDucal Apple Nectar, 5.3 oz cans.Mar 8, 2016

Recent FDA inspections

2 inspections from Jan 7, 2015 to May 11, 2023.

DateSiteProductClassificationFEI
May 11, 2023Miami, FLFood/CosmeticsNo Action Indicated (NAI)3014151436
Jan 7, 2015Miami, FLFood/CosmeticsNo Action Indicated (NAI)3014151436
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.

FacilityLocationInspectionsLatest
FEI 3014151436Miami, FL2May 11, 2023

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