Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 grams. 1package is 14
Summary
The FDA issued a Class II for Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is a by Specialty Bakers, LLC. Reason: Undeclared Allergen (Soy).
Details
Source
Food Recall
External ID
H-1145-2026
Action Date
2026-07-15
Status
Ongoing
Category
food
Product Description
Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 grams. 1package is 142 grams. 1 package has 1 plastic tray which holds 6 desserts shells. Plastic is wrapped around 1 tray. 24 packs/Case. Frozen
Lot/Code Info: Lot Number: 968674
Quantity Affected: 449 cases
Reason for Recall
Undeclared Allergen (Soy)
Distribution
The adulterated product was distributed to the following states, Pennsylvania.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-28
Company
Marysville, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 23 food recalls issued in the same week, part of 81 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Specialty Bakers, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Specialty Bakers, LLC have FDA actions?
This is the only FDA action we have on record for Specialty Bakers, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1145-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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