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
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
- Brand
- Queseria
- 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 2018 | Recall initiated by company | |
| 27 Nov 2018 | Classified by FDA | +18 days |
| 5 Dec 2018 | Published 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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