Class IITerminated in FDA datasetRecall initiated Oct 13, 2018

Corn and Black Bean Blend: Sold in 2 lb. and 25 lb. packages. Brand Name: Jon-Lin¿…

Recalling firm: McCain Foods USA

Why it was recalled

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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 1, 2019.

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ProductCorn and Black Bean Blend: Sold in 2 lb. and 25 lb. packages. Brand Name: Jon-Lin¿ NatureSmart¿; Jon-Lin¿, Chef Sensations¿
Package size2 lb

FDA code information

All products shipped on or after January 1, 2016 Batch numbers: 1002015953 1002309966 1002345874 1002699283 1002755317 1001708561 1001732304 1001574717 1001578943 1001580606 1001582083 1001600074 1001604442 1001605993 1001612423 1001708560 1001709862 1001720219 1001732303 1001741266 1001748288 1001938397 1001574725 1001587733 1001611201 1001673551 1002097061 1002229375 1002428677 1002596746 1002637120 1002666833 1001823845 1001845990 1001968885 1002011220 1001618944 1001642092 1001652776 1001757201 1001758635 1001940019 1001949094 1001950272 1001954292 1001968900 1001975253 1001877723

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Full FDA record and distribution details

Original product description

Corn and Black Bean Blend: Sold in 2 lb. and 25 lb. packages. Brand Name: Jon-Lin¿ NatureSmart¿; Jon-Lin¿, Chef Sensations¿

Original FDA recall 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 details

Recall number
F-0207-2019
Event ID
81281
FDA status
Terminated
Initiated
Oct 13, 2018
Reported
Oct 31, 2018
Classified
Oct 29, 2018
Terminated
Nov 1, 2019
Quantity
94,453 cases
Location
Oakbrook Ter, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

US and Canada, China, Korea and Mexico

FDA source record · F-0207-2019

Data updated September 16, 2026. View official FDA data ↗

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