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Mondelez
Recall · Class II2018-03-13Terminated

Something may have got into the product that should not be there.

Mondelez Global LLC is initiating a recall because remnants of a half peanut shell were found in two containers of bulk candy from a single lot during the repacking process and the candy is not labeled as containing peanuts. Mondelez Global LLC after an investigation, including inspection of product within in their control from the same lot did not find any other evidence of peanut contamination. The firm believes this is most likely to be an isolated incident and that product on the market is unlikely to contain any peanut pieces and the product is not likely to cause adverse health consequences to peanut allergic consumers. No adverse health events have been reported. Never the less, out of an abundance of caution, we have determined to conduct a voluntary recall to the retail level.

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 Mondelez.

What the notice covered

Sour Patch Kids, 1.9 lb bag

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 II means

The FDA’s middle class: use of the product may cause temporary or medically reversible health consequences, and the probability of serious harm is remote.

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-0952-2018
Kind of action
Recall
Dated
2018-03-13
Terminated
2021-08-17
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-0952-2018"

To see it in the FDA’s own words, search the reference number F-0952-2018 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