Class IITerminated in FDA datasetRecall initiated Jan 7, 2026

Gluten Free 14" Seasoned Vegan Pizza Crust

Recalling firm: Rich Products Corp

Why it was recalled

Product contains undeclared milk and egg

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 24, 2026.

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ProductGLUTEN FREE 14" SEASONED VEGAN PIZZA CRUST; INGREDIENTS: WATER, RICE FLOUR, POTATO STARCH, RICE STARCH, TAPIOCA STARCH, CANE SUGAR, MODIFIED RICE STARCH, POTATO FLOUR, PEA FIBER, CONTAINS LESS THAN 2% OF THE FOLLOWING: CANOLA OIL, YEAST, SALT, CELLULOSE GEL, EXTRA VIRGIN OLIVE OIL, GARLIC POWDER, SPICES, XANTHAN GUM, CELLULOSE GUM, CULTURED BROW RICE, BROWN RICE FLOUR, CITRIC ACID, LACTIC ACID; MAY CONTAIN MILK AND EGGS; MANUFACTURED BY VENCE BAKERY; Net Case Wt: 14 LB 6 OZ (6.52 KG); Unit Net Wt: 11.5 OZ (326 G); COUNT: 20; KEEP FROZEN; GTIN code on shipper case (01) 0 0859955 00412 6
Package size14 LB

FDA code information

Product Code 19923 Lot Code/Batch ID 0002979162 Best if Used By: 5/10/26

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Full FDA record and distribution details

Original product description

GLUTEN FREE 14" SEASONED VEGAN PIZZA CRUST; INGREDIENTS: WATER, RICE FLOUR, POTATO STARCH, RICE STARCH, TAPIOCA STARCH, CANE SUGAR, MODIFIED RICE STARCH, POTATO FLOUR, PEA FIBER, CONTAINS LESS THAN 2% OF THE FOLLOWING: CANOLA OIL, YEAST, SALT, CELLULOSE GEL, EXTRA VIRGIN OLIVE OIL, GARLIC POWDER, SPICES, XANTHAN GUM, CELLULOSE GUM, CULTURED BROW RICE, BROWN RICE FLOUR, CITRIC ACID, LACTIC ACID; MAY CONTAIN MILK AND EGGS; MANUFACTURED BY VENCE BAKERY; Net Case Wt: 14 LB 6 OZ (6.52 KG); Unit Net Wt: 11.5 OZ (326 G); COUNT: 20; KEEP FROZEN; GTIN code on shipper case (01) 0 0859955 00412 6

Extracted codes and context

TypeCode / valueContext
best by5/10/26Product Code 19923 Lot Code/Batch ID 0002979162 Best if Used By: 5/10/26

Original FDA recall reason

Product contains undeclared milk and egg

Recall details

Recall number
H-0440-2026
Event ID
98271
FDA status
Terminated
Initiated
Jan 7, 2026
Reported
Feb 11, 2026
Classified
Feb 2, 2026
Terminated
Mar 24, 2026
Quantity
2792 cases
Location
Buffalo, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

CA, IL, GA, AZ, IN, DE

FDA source record · H-0440-2026

Data updated September 16, 2026. View official FDA data ↗

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