Specialty Bakers, LLC Recall: Undeclared Allergen (Soy)
United States
TerminatedClass II
- Company
- Specialty Bakers, LLC
- Product
- Vanilla Dessert Shells (Giant), 6 dessert shells/1 package,…
- Recall date
- May 28, 2026
- Terminated
- August 12, 2026
- Source
- FDA
Reason for recall
Undeclared Allergen (Soy)
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 449 cases | Lot Number: 968674 |
Distribution
- The adulterated product was distributed to the following states
- Pennsylvania.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1145-2026
- Event ID
- 99253
- Status
- Terminated
- Classification
- Class II
- Company
- Specialty Bakers, LLC
- 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
- Quantity
- 449 cases
- Reason
- Undeclared Allergen (Soy)
- Recall initiation date
- May 28, 2026
- Report date
- July 15, 2026
- Classification date
- Not published in this source record
- Termination date
- August 12, 2026
- Distribution pattern
- The adulterated product was distributed to the following states, Pennsylvania.
- UPC, lot, and code information
- Lot Number: 968674
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Specialty Bakers, LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
