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Gretchen's Shoebox Express
Recall · Class II2016-03-02Terminated

Contains cashews without saying so on the label, which matters if you are allergic to it.

The Cheese & Fruit Bistro Boxes are recalled because the product may contain an undeclared cashews.

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 Gretchen's Shoebox Express.

What the notice covered

Cheese & Fruit Bistro Box (Item #11015085), Starbucks brand. Product is packaged in plastic clamshell, net wt. 5.3 oz. The UPC is 7 62111 88146 5.

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-1029-2016
Kind of action
Recall
Dated
2016-03-02
Terminated
2016-09-08
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

Nobody has yet assessed whether this notice concerns the products we track for this company, so it is not shown on product pages.

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-1029-2016"

To see it in the FDA’s own words, search the reference number F-1029-2016 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