Food Recall Check
Class II · Moderate risk Ongoing Initiated Jul 27, 2023 (3 years ago)

BAPS SHAYONA Plain Penda Ricotta fudge discs flavored with rose water recall

Recalled by BAPS Shayona · Lilburn, GA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

During an FDA inspection the firm was notified that some of their products contains undeclared soy.

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

BAPS SHAYONA Plain Penda Ricotta fudge discs flavored with rose water Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53152 Contains: Milk, Nut

Quantity: 723 units

Food: Cheese

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

A06G2723 Best By 09/25/2023, A12G1323 Best By 9/11/2023, A06G0523 Best By 9/3/2023, A05F1423 Best By 8/13/2023, A04F0823 Best By 8/7/2023, A12E1723 Best By 7/16/2023

Where it was sold

Alabama Florida Georgia North Carolina South Carolina Tennessee

FDA's distribution note: Product was shipped to the following states: AL, FL, GA, NC, SC & TN

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern.

Recalling firm
BAPS Shayona
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 27, 2023
In FDA report of
Dec 13, 2023
FDA recall number
F-0488-2024 · event 92774
Official record
FDA enforcement report search

Also recalled with it (12 more products)

FDA files each product of one recall action separately; these share the same FDA event.