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Stop using now Food recall · FDA · Published May 28, 2026

Specialty Bakers Recalls Vanilla Dessert Shells Due to Undeclared Soy

Specialty Bakers, LLC is recalling Frozen Vanilla Dessert Shells (Giant) because they contain an undeclared allergen: soy. Check your freezer.

🇺🇸 FDA recall #H-1145-2026FoodSpecialty Bakers ›
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Contact the company

Recalling firmSpecialty Bakers, LLC450 S State Rd · Marysville, PA 17053-1020
✎ GovInfoNow plain-language explainer

What happened, in plain English

Specialty Bakers, LLC has recalled Frozen Vanilla Dessert Shells (Giant) because the product contains an undeclared allergen: soy. This poses a risk to individuals with soy allergies who may not be aware of its presence. The recall affects products distributed in Pennsylvania. Read more at govinfonow.com/recall/6197-specialty-bakers-recalls-vanilla-dessert-shells-due-to-undeclared-soy.

Source Summary by GovInfoNow · govinfonow.com/recall/6197-specialty-bakers-recalls-vanilla-dessert-shells-due-to-undeclared-soy · Updated October 9, 2026 · Official notice: FDA #H-1145-2026

Cite this page

“Specialty Bakers Recalls Vanilla Dessert Shells Due to Undeclared Soy.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6197-specialty-bakers-recalls-vanilla-dessert-shells-due-to-undeclared-soy. Based on FDA recall #H-1145-2026.

Why it’s dangerous

The product contains soy, which is not listed on the label. For people with soy allergies, consuming even a small amount can trigger a serious or life-threatening allergic reaction.

Who’s affected

Consumers in Pennsylvania who purchased Frozen Vanilla Dessert Shells (Giant) containing soy are at risk of an allergic reaction. Individuals with known soy allergies are the primary group affected by this undeclared ingredient.

How to tell if you have this one

Look for Frozen Vanilla Dessert Shells (Giant) in plastic trays wrapped in plastic, containing 6 dessert shells per package. Check for Lot Number 968674 on the packaging. The product was distributed to Pennsylvania.

  • Brand
    Specialty Bakers
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Vanilla Dessert Shells (Giant) if you have them in your possession.

  2. Check for lot number 968674

    Verify if your package has Lot Number 968674 to confirm it is part of the recall.

  3. Discard or return the product

    The record does not specify a remedy, so please contact Specialty Bakers, LLC for instructions on disposal or refund.

Where it went and when

Where it was distributed

Distributed in Pennsylvania.

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: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew 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: “The adulterated product was distributed to the following states, Pennsylvania.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Pennsylvania.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: May 28, 202612. FDA classified it Class II: Jul 7, 202623. Published in FDA’s Enforcement Report: Jul 15, 202634. FDA terminated the recall: Aug 12, 202642026
  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.

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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 #H-1145-2026 (May 28, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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