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Lower risk Food recall · FDA · Published April 11, 2018

Sugarfina Platinum Bling Ring Recall: Undeclared Fish Gelatin Allergen

Sugarfina recalls Platinum Bling Rings due to undeclared fish gelatin in ingredients. This poses a risk for people with fish allergies. Consumers should check product details and contact Sugarfina for guidance.

🇺🇸 FDA recall #F-1397-2018FoodSugarfina ›
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Contact the company

Recalling firmSugarfina, LLC3915 W 102nd St · Inglewood, CA 90303-1004
✎ GovInfoNow plain-language explainer

What happened, in plain English

Sugarfina is recalling its Platinum Bling Rings because they contain fish gelatin that wasn't listed on the ingredient or allergen information. This could cause allergic reactions in people who are sensitive to fish. The recall is for specific product models sold with a particular UPC code. Read more at govinfonow.com/recall/19223-sugarfina-platinum-bling-ring-recall-undeclared-fish-gelatin-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/19223-sugarfina-platinum-bling-ring-recall-undeclared-fish-gelatin-allergen · Updated October 7, 2026 · FDA enforcement record: FDA #F-1397-2018

Cite this page

“Sugarfina Platinum Bling Ring Recall: Undeclared Fish Gelatin Allergen.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19223-sugarfina-platinum-bling-ring-recall-undeclared-fish-gelatin-allergen. Based on FDA recall #F-1397-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1397-2018%22&limit=1).

Why it’s dangerous

The rings contain fish gelatin that wasn't listed on the ingredient or allergen information. This means individuals with fish allergies could react to the gelatin if they consume the product. The gelatin is part of the product's ingredients but wasn't declared as an allergen.

Who’s affected

People who own or use Sugarfina Platinum Bling Rings with the specific SKU and UPC code are affected. Those with fish allergies are at higher risk due to the undeclared gelatin.

How to tell if you have this one

Check for the product SKU R-1790 and UPC 840278116139 on the ring packaging. The rings are sold in the U.S. and made in Greece.

  • Brand
    Sugarfina
  • Product
    Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the SKU R-1790 and UPC 840278116139 on the ring packaging to confirm it is the recalled product.

Where it went and when

Where it was distributed

Distributed in 16 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “FL, AR, OR, UT, PA, CA, NJ, MA,NY, MD, IL, IN,SC, TN, LA, GA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

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

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Apr 11, 201812. FDA classified it Class III: May 9, 201823. Published in FDA’s Enforcement Report: May 16, 201834. FDA terminated the recall: Sep 14, 201842018
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1397-2018 (April 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1397-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA