CLASS II Food recall · Reported 11 Jun 2025 · FDA Enforcement Report

Salsa Cilantro plastic jugs packaged 4 jugs to case recalled

Mexquisite is recalling Salsa Cilantro plastic jugs packaged 4 jugs to case, distributed in California, Texas. The recall was initiated on 25 Apr 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesMSC12114
Quantity recalled339 cases

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
H-0001-2025
FDA event ID
96899
Recalling firm
Mexquisite, San Antonio, TX
Classification
Class II
Status
Terminated
Recall initiated
25 Apr 2025
FDA classified
3 Jun 2025
Reported
11 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Dips & Spreads

Timeline

25 Apr 2025Recall initiated by company
3 Jun 2025Classified by FDA+39 days
11 Jun 2025Published 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

Potential foreign object contamination

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Salsa Cilantro 8.5lb plastic jugs packaged 4 jugs to case. MSC12114

Where it was distributed

Texas and California

CaliforniaTexas

Questions about this recall

Why was it recalled?

Potential foreign object contamination

Which lots are affected?

MSC12114

Where was it sold?

Texas and California

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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