Fresh Recalls

FDAClass I · Food · Recall H-1220-2026 · Recalled August 12, 2026

Requeson recall — La Colonia Foods Llc

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Requeson
Company / brand
La Colonia Foods
Lot / serial / date codes
Lact1032
Distribution
The recalled product was distributed to the following states: MD, VA
Agency product description and boundaries

Requeson, bulk product from Clover Hill Dairy packed into a plastic 18-lb bucket. Unknown labeling information. Keep refrigerated.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Products may be contaminated with Listeria monocytogenes.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Requeson

3. Open the official notice or contact

Official recall ID
H-1220-2026
Brand
La Colonia Foods
Classification
Class I
Units affected
19 (18-lb bucket) units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Rockville, MD, United States
Firm address
7300 Westmore Rd Ste 3, Ste 3, 20850-5223

Identifying details (verbatim from the notice)

Product codes / lots
Lact1032
Distribution
The recalled product was distributed to the following states: MD, VA
Firm notified the public via
E-Mail
FDA event ID
99325
Recall initiated
June 4, 2026
FDA classified
August 4, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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