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Hidroponicos Brownia, S.P.R. de R.L. 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

United States

TerminatedClass I

Company
Hidroponicos Brownia, S.P.R. de R.L.
Product
Aztlan Mole Oaxaqueno Negro; 10 kg plastic buckets (22 lbs)…
Recall date
August 17, 2018
Terminated
February 5, 2019
Source
FDA

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 Not published in this source record 450 x 10 kg barrels Mole Oaxaqueno Negro: lots 3750, 3765, 3936, 3989.

Distribution

  • California

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1981-2018
Event ID
80955
Status
Terminated
Classification
Class I
Company
Hidroponicos Brownia, S.P.R. de R.L.
Product description
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
Quantity
450 x 10 kg barrels
Reason
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
Recall initiation date
August 17, 2018
Report date
September 19, 2018
Classification date
Not published in this source record
Termination date
February 5, 2019
Distribution pattern
California
UPC, lot, and code information
Mole Oaxaqueno Negro: lots 3750, 3765, 3936, 3989.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 80955 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Hidroponicos Brownia, S.P.R. de R.L.

Product
Aztlan Mole Poblano; 10 kg plastic buckets (22 lbs); Ing…
Published
September 19, 2018
Distribution
California

View recall →

Responsible company: Hidroponicos Brownia, S.P.R. de R.L.

Other recalls from Hidroponicos Brownia, S.P.R. de R.L.

FDA Recall United States Terminated Historical recordClass I

Hidroponicos Brownia, S.P.R. de R.L.

Product
Aztlan Mole Poblano; 10 kg plastic buckets (22 lbs); Ing…
Published
September 19, 2018
Distribution
California

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.