CLASS I Food recall · Reported 5 Dec 2018 · FDA Enforcement Report

Queseria "La Milagrosa" La Delicia al Paladar recalled

Alebrije Imports is recalling Queseria "La Milagrosa" La Delicia al Paladar. The recall was initiated on 9 Nov 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo codes on packages
Quantity recalled426 kgs. (937 (total)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0664-2019
FDA event ID
81551
Recalling firm
Alebrije Imports, Los Angeles, CA
Classification
Class I
Status
Terminated
Recall initiated
9 Nov 2018
FDA classified
27 Nov 2018
Reported
5 Dec 2018
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella
Product category
Other

Timeline

9 Nov 2018Recall initiated by company
27 Nov 2018Classified by FDA+18 days
5 Dec 2018Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

California Department of Food and Agriculture sampled and found Salmonella in cheese imported from Mexico.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Queseria "La Milagrosa" La Delicia al Paladar. 1/2 kg and 1 kg sizes. Packaged in a plastic bag with a yellow label.

Where it was distributed

Los Angeles area only

Questions about this recall

Why was it recalled?

California Department of Food and Agriculture sampled and found Salmonella in cheese imported from Mexico.

Which lots are affected?

No codes on packages

Where was it sold?

Los Angeles area only

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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