McCain Foods USA Recall: During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.

🇺🇸 United States

1. October 13, 2018 - Recall initiated
2. October 31, 2018 - Reported by source
3. November 1, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0323-2019

Event ID

81281

Status

Terminated

Classification

Class II

Company

McCain Foods USA

Product description

Fire-Roasted Home-Style Yellow Pepper Strips;: Sold in 20 lb. containers. Brand Name: Jon-Lin¿

Quantity

1,622 cases

Reason

During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.

Recall initiation date

October 13, 2018

Report date

October 31, 2018

Classification date

Not published in this source record

Termination date

November 1, 2019

Distribution pattern

US and Canada, China, Korea and Mexico

UPC, lot, and code information

All products shipped on or after January 1, 2016 Batch numbers: 1002497593 1002789531 1001920995 1002235524 1002497593 1002747079 1002789531 1001920995

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

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 81281 with 9 other product entries in Public Health Trace.

Responsible company: McCain Foods USA

Other recalls from McCain Foods USA

Where this information comes from

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

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

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: July 18, 2026 ET

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.

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