Food Recall Check
Class III · Low risk Terminated Initiated Apr 11, 2018 (8 years ago)

Sugarfina Platinum Bling Ring recall

Recalled by Sugarfina, LLC · Inglewood, CA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

Undeclared allergen: Fish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 1,342 units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

No codes

Where it was sold

Arkansas California Florida Georgia Illinois Indiana Louisiana Massachusetts Maryland New Jersey New York Oregon Pennsylvania South Carolina Tennessee Utah

FDA's distribution note: FL, AR, OR, UT, PA, CA, NJ, MA,NY, MD, IL, IN,SC, TN, LA, GA.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to fish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Sugarfina, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 11, 2018
In FDA report of
May 16, 2018
Terminated
Sep 14, 2018
FDA recall number
F-1397-2018 · event 79966
Official record
FDA enforcement report search

Other recalls by Sugarfina, LLC