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Yost Foods, Inc Recall: Product tested positive for Listeria monocytogenes.

United States

TerminatedClass I

Company
Yost Foods, Inc
Product
Aji Amarillo Paste, in 40 lb buckets.
Recall date
March 11, 2019
Terminated
December 27, 2019
Source
FDA

Reason for recall

Product tested positive for Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Aji Amarillo Paste, in 40 lb buckets. Not published in this source record 1000 lbs Lot Y05319

Distribution

  • Distributed to one customer in Ohio.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1309-2019
Event ID
82632
Status
Terminated
Classification
Class I
Company
Yost Foods, Inc
Product description
Aji Amarillo Paste, in 40 lb buckets.
Quantity
1000 lbs
Reason
Product tested positive for Listeria monocytogenes.
Recall initiation date
March 11, 2019
Report date
May 8, 2019
Classification date
Not published in this source record
Termination date
December 27, 2019
Distribution pattern
Distributed to one customer in Ohio.
UPC, lot, and code information
Lot Y05319
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Yost Foods, Inc

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.