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DESHI DISTRIBUTORS, LLC

FDA Regulatory Profile

DESHI DISTRIBUTORS, LLC has 1 FDA recall (1 Class I), 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "DESHI DISTRIBUTORS, LLC" and its spelling variant "Deshi Distributors".

Latest recall
F-1442-2019 · Class I · May 9, 2019
Latest inspection
Mar 17, 2026 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1 (1 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

DESHI DISTRIBUTORS, LLC: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 1 inspections120222023: 0 inspections020232024: 0 inspections020242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202400000
202300000
202210000
202110000
202000000
201900011
201800000
201700000

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

1 recall record on May 9, 2019.

NumberClassProductDate
F-1442-2019Class IDeshi Golden Raisin, packaged in 3.5 oz, 7 oz. and 14 oz. clear plasticMay 9, 2019

Recent FDA inspections

3 inspections from Aug 25, 2021 to Mar 17, 2026.

DateSiteProductClassificationFEI
Mar 17, 2026Jamaica, NYFood/CosmeticsVoluntary Action Indicated (VAI)3013235786
Sep 12, 2022Jamaica, NYFood/CosmeticsVoluntary Action Indicated (VAI)3013235786
Aug 25, 2021Jamaica, NYFood/CosmeticsVoluntary Action Indicated (VAI)3013235786
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 3013235786Jamaica, NY3Mar 17, 2026

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FDA data resources

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