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Lower risk Food recall · FDA · Published April 22, 2019

Island Desserts Key Lime Torte Recall: Undeclared Food Dyes

Island Desserts Llc DBA Pastry Art recalls Key Lime and Cream Torte due to undeclared FD&C colors. Products sold after 10/18/2018 may contain Yellow #5 and Blue #1.

🇺🇸 FDA recall #F-1332-2019FoodIsland Desserts ›
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Recalling firmIsland Desserts Llc DBA Pastry Art24 Walpole Park South · Walpole, MA 02081-2541
✎ GovInfoNow plain-language explainer

What happened, in plain English

Island Desserts is recalling Key Lime and Cream Torte products because they contain undeclared food dyes. This could pose health risks for people with allergies to these dyes. Read more at govinfonow.com/recall/17558-island-desserts-key-lime-torte-recall-undeclared-food-dyes.

Source Summary by GovInfoNow · govinfonow.com/recall/17558-island-desserts-key-lime-torte-recall-undeclared-food-dyes · Updated October 5, 2026 · FDA enforcement record: FDA #F-1332-2019

Cite this page

“Island Desserts Key Lime Torte Recall: Undeclared Food Dyes.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17558-island-desserts-key-lime-torte-recall-undeclared-food-dyes. Based on FDA recall #F-1332-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1332-2019%22&limit=1).

Why it’s dangerous

The product contains undeclared FD&C colors Yellow #5 and Blue #1. These dyes are not listed on the product label, which could cause allergic reactions in sensitive individuals.

Who’s affected

People who purchased Key Lime and Cream Torte from Island Desserts after October 18, 2018. Those with allergies to Yellow #5 or Blue #1 dyes are most at risk.

How to tell if you have this one

Check for Key Lime and Cream Torte, 5 oz. products delivered after October 18, 2018. The product is labeled as 'Keep in Freezer for up to 6 months or refrigerated for 5 days'.

  • Brand
    Island Desserts
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name and delivery date on the label to confirm if it was purchased after October 18, 2018.

Where it went and when

Where it was distributed

Distributed in Massachusetts and Rhode Island.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: yesRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “MA and RI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Massachusetts, Rhode Island.

Recall timeline

FDA terminated this recall 51 days after the firm started it.

1. Firm started the recall: Apr 22, 201912. FDA classified it Class II: May 8, 201923. Published in FDA’s Enforcement Report: May 15, 201934. FDA terminated the recall: Jun 12, 201942019
  1. Firm started the recall
  2. FDA classified it Class II
  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.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury from this product?

No, the recall is for health reasons related to potential allergic reactions, not physical injury risks.

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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-1332-2019 (April 22, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1332-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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