Crumbled Cotija Net Wt
Reason Product has the potential to be contaminated with Listeria monocytogenes.
Classic Castle Brand Shredded Three Cheese Blend recall
Recalled by Castle Importing, Inc. · Fontana, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product has the potential to be contaminated with Listeria monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Classic Castle Brand Shredded Three Cheese Blend Net Wt. 20 Lbs, Net Wt. 5 lbs. Fontana, CA 92336 Plant #06-00333
Quantity: 667 cases
Food: Cheese
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
CA SHR 3 CHS BLND 4/5lbs 00754-2-24IN4/5 70095 Customer Lot # 23290 23312 23325 23354 23354 23355 24003 24033
Where it was sold
California Connecticut Florida Illinois Ohio Texas Washington
FDA's distribution note: U.S. distribution to the following: CA< OH, CT, FL, TX, WA, IL No foreign distribution.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Castle Importing, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 5, 2024
- In FDA report of
- Mar 13, 2024
- Terminated
- May 6, 2025
- FDA recall number
- F-1039-2024 · event 94117
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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