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Sugarfina
Recall · Class III2018-04-11Terminated

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

Internal audit discovered that their Platinum Bling Ring product contains fish gelatin that is not declared on the ingredient or allergen information

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 Sugarfina.

What the notice covered

Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark chocolate, these interlocking rings have a thin sugar shell brushed with edible silver: Ingredients: Dark Chocolate (cocoa, sugar, cocoa butter, soy lecithin (an emulsifier_ sugar, Dextrose, gum Arabic, color added, gelatin. Made in Greece Distributed by Sugarfina Inc. Santa Monica Blvd., Beverly Hills, CA

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 III means

The FDA’s least serious class: use of the product is not likely to cause adverse health consequences. Often a labelling or packaging fault.

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-1397-2018
Kind of action
Recall
Dated
2018-04-11
Terminated
2018-09-14
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-1397-2018"

To see it in the FDA’s own words, search the reference number F-1397-2018 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