CLASS I Food recall · Reported 19 Sep 2018 · FDA Enforcement Report

Aztlan Mole Oaxaqueno Negro recalled by Hidroponicos Brownia, S.P.R.

Hidroponicos Brownia S.P.R. de R.L is recalling Aztlan Mole Oaxaqueno Negro, distributed in California. The recall was initiated on 17 Aug 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesMole Oaxaqueno Negro: lots 3750, 3765, 3936, 3989.
Quantity recalled450 x 10 kg barrels

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-1981-2018
FDA event ID
80955
Recalling firm
Hidroponicos Brownia S.P.R. de R.L, Ciudad De Mexico, N/A
Classification
Class I
Status
Terminated
Recall initiated
17 Aug 2018
FDA classified
24 Sep 2018
Reported
19 Sep 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Flour

Timeline

17 Aug 2018Recall initiated by company
19 Sep 2018Published in enforcement report+33 days
24 Sep 2018Classified by FDA+5 days

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

Reason for recall

During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen statement

Product as listed by the FDA

Aztlan Mole Oaxaqueno Negro; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, peanut, soybean oil, pasilla pepper, guajillo pepper, sesame seed, cookie, cocoa, corn flour, idozided salt, condiments and spices. Sodium benzoate as a preservative. Distributed by/distributed for: Jelley Crown Inc. City of Industry, CA

Where it was distributed

California

California

Questions about this recall

Why was it recalled?

During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen statement

Which lots are affected?

Mole Oaxaqueno Negro: lots 3750, 3765, 3936, 3989.

Where was it sold?

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 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.

Other products in this recall event

1 other product · FDA event 80955

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