RecallHawk
Class I Recall

Selectos Latinos Requeson Mexicano Mexican Cottage Cheese, Net Weight 16 oz, packed into retail-sized clear plastic cont

La Colonia Foods Llc

Summary

The FDA issued a Class I for Selectos Latinos Requeson Mexicano Mexican Cottage Cheese, Net Weight 16 oz, pac by La Colonia Foods Llc. Reason: Products may be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

H-1219-2026

Action Date

2026-08-12

Status

Ongoing

Category

food

Product Description

Selectos Latinos Requeson Mexicano Mexican Cottage Cheese, Net Weight 16 oz, packed into retail-sized clear plastic containers. Keep refrigerated.

Lot/Code Info: Selec1011

Quantity Affected: 169 (16-oz) units

Reason for Recall

Products may be contaminated with Listeria monocytogenes.

Distribution

The recalled product was distributed to the following states: MD, VA

Type: Voluntary: Firm initiated

Recall Initiated: 2026-06-04

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 36 food recalls issued in the same week, part of 73 food-related FDA actions this month.

La Colonia Foods Llc has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (La Colonia Foods Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does La Colonia Foods Llc have FDA actions?

La Colonia Foods Llc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1219-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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