SLR FOOD Distribution, Inc.

FDA Regulatory Profile

SLR FOOD Distribution, Inc. has 3 FDA recalls (1 Class I), 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "SLR FOOD Distribution, Inc." and its spelling variant "Slr Food Distribution".

Latest recall
H-0070-2026 · Class II · Sep 26, 2025
Latest inspection
Nov 15, 2023 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls3 (1 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

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

SLR FOOD Distribution, 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
202500010
202400000
202310010
202200000
202100000
202000000
201900000
201800011
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

3 recall records from Oct 10, 2018 to Sep 26, 2025.

NumberClassProductDate
H-0070-2026Class IIWise Wife Ground CinnamonSep 26, 2025
F-1602-2023Class IIIDried LongansSep 5, 2023
F-0341-2019Class ISUGAR MELON CANDY / WAX GOURD The product comes in a 7.04oz plastics package marked with barcode…Oct 10, 2018

Recent FDA inspections

1 inspection on Nov 15, 2023.

DateSiteProductClassificationFEI
Nov 15, 2023Hicksville, NYFood/CosmeticsNo Action Indicated (NAI)3014780444
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 3014780444Hicksville, NY1Nov 15, 2023

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