Quesos La Ricura, Ltd. FDA Inspection Record

FEI 3003555719 · Inspections, Form 483s, warning letters and import refusals

Quesos La Ricura, Ltd. is an FDA-inspected facility (FEI 3003555719) located in Hicksville, NY, US. RegDataLab tracks 11 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 17, 2025: Voluntary Action Indicated (VAI)
Inspections on record
11 (7 VAI, 4 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
3, latest Jan 25, 2022

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

Showing the 10 most recent of 11 inspections. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 17, 2025Voluntary Action Indicated (VAI)Sanitation preventive controls - Implement (21 CFR 117.135(a)(1))
Hazard analysis - Identification of hazard (21 CFR 117.130(a)(1))
Importer verification (21 CFR 123.12(a)(2))
Aug 23, 2023Voluntary Action Indicated (VAI)Hazard analysis - Identification of hazard (21 CFR 117.130(a)(1))
HACCP training or qualification (21 CFR 123.10)
Importer verification (21 CFR 123.12(a)(2))
Jan 31, 2020No Action Indicated (NAI)No citations listed
Feb 1, 2019No Action Indicated (NAI)Plant construction and design (21 CFR 117.20(b))
Plant operations - Precautions (21 CFR 117.80(a))
Feb 4, 2016Voluntary Action Indicated (VAI)Floors, walls and ceilings (21 CFR 110.20(b)(4))
Drip and condensate (21 CFR 110.20(b)(4))
Cleaning and sanitizing operations (21 CFR 110.35(a))
As source of contamination (21 CFR 110.37(b)(3))
and 4 more
Nov 26, 2013Voluntary Action Indicated (VAI)Cleaning and sanitizing operations (21 CFR 110.35(a))
As source of contamination (21 CFR 110.37(b)(3))
Jan 17, 2013Voluntary Action Indicated (VAI)Drip and condensate (21 CFR 110.20(b)(4))
Storage requirements (21 CFR 110.35(b)(2))
Aug 8, 2012Voluntary Action Indicated (VAI)Work-in-progress (21 CFR 110.80(b)(5))
Sep 10, 2010Voluntary Action Indicated (VAI)Drip and condensate (21 CFR 110.20(b)(4))
Safe and adequate for use (21 CFR 110.35(d)(5))
Apr 16, 2010No Action Indicated (NAI)No citations listed

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
Jan 25, 2022Class IIF-0733-2022Quesos La Ricura Mi Ranchito Fresh Cheese with Hot Peppers, 14. 0z.
May contain elevated levels of coliform
Jan 24, 2020Class IF-0598-2020QUESOS LA RICURA brand Queso Cotija; Cotija Cheese; AGED OVER 60 DAYS; Ingredients: Raw…
Possible contamination with Shiga toxin-producing E. coli (STEC).
Apr 8, 2010Class IIIF-2228-2010Quesos La Ricura brand Chunky Cheese, Net Wt. 16 OZ. (454g), UPC 7 69087 00002 9…
Positive phosphatase finding in Chunky Cheese based on sampling and analysis by New York State Department of Agriculture & Markets' Division…

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 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 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Quesos La Ricura, Ltd.
Location
Hicksville, NY (US)
Source
inspections

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