Reference Source

Agricola Boui, S.A. de C.V. · 99-23 · MEXICO

For Agricola Boui, S.A. de C.V., import alert is 99-23; country is MEXICO; import alert name is Detention Without Physical Examination of Produce Due to Contamination With Human Pathogens; product is Squash | Cucumbers (Persian/Slicer); product code is 24 F - - 06 Squash, Summer (Fruit Used as Vegetable) | 24 F - - 20 Cucumbers (Fruit Used as Vegetable); date published is 12/30/2013; address is Allende No. 823 Ote. Local 18 , Leon, Sonora MEXICO, verified against its source on 2026-09-30.

Firm
Agricola Boui, S.A. de C.V. verified
Import alert
99-23
Import alert name
Detention Without Physical Examination of Produce Due to Contamination With Human Pathogens
Country
MEXICO verified
Address
Allende No. 823 Ote. Local 18 , Leon, Sonora MEXICO verified
Date published
12/30/2013 verified
Product code
24 F - - 06 Squash, Summer (Fruit Used as Vegetable) | 24 F - - 20 Cucumbers (Fruit Used as Vegetable) each item verified
Product
Squash | Cucumbers (Persian/Slicer) each item verified
FDA notes
SALMONELLA; | Two positive samples from two different entry samples; SWID 984477 and 986593 | SALMONELLA; each item verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

Agricola Boui, S.A. de C.V. Date Published : 12/30/2013 Allende No. 823 Ote. Local 18 , Leon, Sonora MEXICO

— accessdata.fda.gov, retrieved 2026-09-15

Where each value comes from

The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.

Product code, Product and FDA notes

24 F - - 06 Squash, Summer (Fruit Used as Vegetable) Date Published: 12/30/2013 Desc: Squash Problems: SALMONELLA; 24 F - - 20 Cucumbers (Fruit Used as Vegetable) Date Published: 12/12/2016 Desc: Cucumbers (Persian/Slicer) Notes: Two positive samples from two different entry samples; SWID 984477 and 986593 Problems: SALMONELLA;

— all from accessdata.fda.gov, retrieved 2026-09-15

Source

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