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The Pictsweet Company
Recall · Class I2016-04-09Terminated

May contain listeria, a germ that can cause serious illness.

Products contain onions which were recalled for the possibility of Listeria monocytogenes contamination.

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming The Pictsweet Company.

What the notice covered

Frozen chopped onions labeled as: a) Kroger(R) CHOPPED ONIONS, RECIPE BEGINNINGS(R), NET WT 12 OZ (340g), UPC 11110 89791, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202 b) PICTSWEET(R) Chopped Onions, recipe helper, NET WT 10 OZ (283g), UPC 70560 96609, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class I means

The FDA’s most serious class: a reasonable probability that using the product will cause serious health consequences or death.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-1655-2016
Kind of action
Recall
Dated
2016-04-09
Terminated
2017-08-03
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

We have not matched this notice to any product in our database — usually because it named no barcode we hold. Products may still have been affected.

How we are treating it

This notice concerns the product line itself or how it was produced.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-1655-2016"

To see it in the FDA’s own words, search the reference number F-1655-2016 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site