CLASS I Food recall · Reported 4 Mar 2015 · FDA Enforcement Report

Sour Cream/Crema Agria is recalled by Queseria Bendita

Queseria Bendita is recalling Sour Cream/Crema Agria is, distributed in Oregon, Washington. The recall was initiated on 16 Jan 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNone
Quantity recalledundetermined because firm does not keep record

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-1368-2015
FDA event ID
70296
Recalling firm
Queseria Bendita, Yakima, WA
Brand
Sour
Classification
Class I
Status
Terminated
Recall initiated
16 Jan 2015
FDA classified
26 Feb 2015
Reported
4 Mar 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Listeria
Product category
Sour Cream

Timeline

16 Jan 2015Recall initiated by company
26 Feb 2015Classified by FDA+41 days
4 Mar 2015Published in enforcement report+6 days

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

Reason for recall

Sour Cream/Crema Agria is recalled because of a potential to be contaminated with Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Sour Cream/Crema Agria is packaged in a plastic tub, Net Wt. 1 lb. The UPC is 0 94922 10608 7.

Where it was distributed

distributed in Oregon and Washington

OregonWashington

Questions about this recall

Is Sour Cream/Crema Agria is recalled?

Yes. Queseria Bendita recalled Sour Cream/Crema Agria is on 16 Jan 2015. The recall is Class I and its status is Terminated. Recall number F-1368-2015.

Why was it recalled?

Sour Cream/Crema Agria is recalled because of a potential to be contaminated with Listeria monocytogenes.

Which lots are affected?

None

Where was it sold?

distributed in Oregon and Washington

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 21 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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