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McCain Foods USA Recall: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

United States

TerminatedClass II

Company
McCain Foods USA
Product
Breaded stuffed Jalapenos poppers labeled in part: Anchor br…
Recall date
July 12, 2016
Terminated
April 22, 2019
Source
FDA

Reason for recall

Firm used Flour from General Mills that has been contaminated with E. Coli O121.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta Bold Poppers, breaded stuffed jalapenos, keep frozen. The product is packaged in a green 4 lb. box with white, green and orange lettering. Not published in this source record Not published in this source record Not published in this source record

Distribution

  • Nationwide. There are no foreign consignees.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2097-2016
Status
Terminated
Classification
Class II
Company
McCain Foods USA
Product description
Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta Bold Poppers, breaded stuffed jalapenos, keep frozen. The product is packaged in a green 4 lb. box with white, green and orange lettering.
Quantity
Not published in this source record
Reason
Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recall initiation date
July 12, 2016
Report date
September 14, 2016
Classification date
Not published in this source record
Termination date
April 22, 2019
Distribution pattern
Nationwide. There are no foreign consignees.
UPC, lot, and code information
Not published in this source record
Voluntary or mandated
Not published in this source record
Initial notification method
Not published in this source record
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: McCain Foods USA

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Product
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Published
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Distribution
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Published
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Distribution
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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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.