Fresh Recalls

FDAClass II · Food · Recall H-1145-2026 · Recalled July 15, 2026

Vanilla Dessert Shells (Giant) recall — Specialty Bakers, LLC

Agency report date: July 15, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Vanilla Dessert Shells (Giant)
Company / brand
Specialty Bakers
Lot / serial / date codes
Lot Number: 968674
Distribution
The adulterated product was distributed to the following states, Pennsylvania.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Undeclared Allergen (Soy)

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Vanilla Dessert Shells (Giant)

3. Open the official notice or contact

Official recall ID
H-1145-2026
Brand
Specialty Bakers
Classification
Class II
Units affected
449 cases
Recall status
Terminated
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Marysville, PA, United States
Firm address
450 S State Rd, N/A, 17053-1020

Identifying details (verbatim from the notice)

Product codes / lots
Lot Number: 968674
Distribution
The adulterated product was distributed to the following states, Pennsylvania.
Firm notified the public via
E-Mail
FDA event ID
99253
Recall initiated
May 28, 2026
FDA classified
July 7, 2026
FDA report date
July 15, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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