ZIYAD BROTHERS IMPORTING FDA Inspection Record

FEI 1461058 · Inspections, Form 483s, warning letters and import refusals

ZIYAD BROTHERS IMPORTING is an FDA-inspected facility (FEI 1461058) located in Cicero, IL, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 9, 2026: Voluntary Action Indicated (VAI)
Inspections on record
7 (4 VAI, 3 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
7, latest Feb 15, 2025
Import refusals
1

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Mar 9, 2026Voluntary Action Indicated (VAI)Develop FSVP (21 CFR 1.502(a))
Identification - entry (21 CFR 1.509(a))
Apr 24, 2023Voluntary Action Indicated (VAI)Food safety plan (21 CFR 117.126(a)(1))
Oct 10, 2019Voluntary Action Indicated (VAI)Food safety plan (21 CFR 117.126(a)(1))
Hazard Analysis - Identification of Hazard (21 CFR 117.130(a)(1))
Nov 13, 2017No Action Indicated (NAI)No citations listed
Feb 17, 2015No Action Indicated (NAI)No citations listed
May 15, 2012Voluntary Action Indicated (VAI)Holding, conveying, mfg systems - design & construction (21 CFR 110.40(d))
Precluding contaminants (21 CFR 110.40(a))
Metal / extraneous materials (21 CFR 110.80(b)(8))
Storage (21 CFR 110.80(a)(1))
and 1 more
Jul 20, 2009No Action Indicated (NAI)Buildings/good repair (21 CFR 110.35(a))
Safe and adequate for use (21 CFR 110.35(d)(5))
Running water at suitable temperature (21 CFR 110.37(e))
Backflow prevention (21 CFR 110.37(b)(5))
and 2 more

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Feb 15, 2025Class IF-0630-2025Ulker Kekstra Mini strawberry, item 3792, 5.3oz foil pack, 10 per case, UPC 8690766082307 and 5 more products
Milk not declared as the major food allergen source for the ingredient Whey
Jul 7, 2023Class IIF-1305-2023Ziyad Brand Jameed Soup Starter sold in a 35.2 fluid ounce tetra pak container with UPC…
Does not declare the major food allergen "milk"
Apr 25, 2023Class IIF-0830-2023Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12…
Elevated levels of lead
May 17, 2018Class IF-1495-2018Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars
Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8 oz. 16 oz., 1/2 gallon and 32 oz. sizes due to potential…
May 20, 2005Class IF-469-5Gandour Sons Halva Plain; a vanilla flavored soft candy made from sugar, tahini (sesame… and 5 more products
Contamination with Salmonella sp.
May 19, 2005Class IF-424-5Ghandour Tahina Extra Sesame Butter, Ingredients: 100% Crushed Sesame Seeds; Distributed…
Contamination with Salmonella Senftenberg, Salmonella Cubana, and Salmonella Idikan.
Apr 12, 2005Class IF-281-5Ziyad Brand Imported Tahini; sesame seed paste packaged in 16 oz., 32 oz. (12 jars per… and 1 more product
The product was found positive for Salmonella Senftenberg by the Minnesota Dept. of Agriculture and the Illinois Dept. of Public Health.

FDA record score

35 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

11 records behind this number
RecordDatePoints x age weightAdds
Class I recall F-0630-2025, this FEI as the recalling firmFeb 15, 202515 x 115
Inspection classified VAIMar 9, 20266 x 16
Class I recall F-1495-2018, this FEI as the recalling firmMay 17, 201815 x 0.253.8
Inspection classified VAIApr 24, 20236 x 0.63.6
Class II recall F-1305-2023, this FEI as the recalling firmJul 7, 20234 x 0.62.4
Class II recall F-0830-2023, this FEI as the recalling firmApr 25, 20234 x 0.62.4
Inspection classified VAIOct 10, 20196 x 0.251.5
Inspection classified VAIMay 15, 201210 years or older, so it adds no points0
Class I recall F-469-5, this FEI as the recalling firmMay 20, 200510 years or older, so it adds no points0
Class I recall F-424-5, this FEI as the recalling firmMay 19, 200510 years or older, so it adds no points0
Class I recall F-281-5, this FEI as the recalling firmApr 12, 200510 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 15, 2026Newest record Nov 5, 2026Current

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Facility details

Company
Global Market Foods LLC F/K/A Ziyad Brothers Importing LLC
Location
Cicero, IL (US)
Source
inspections

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