BAPS SHAYONA Kesar Penda Ricotta fudge discs flavored with saffron Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047
Summary
The FDA issued a Class II for BAPS SHAYONA Kesar Penda Ricotta fudge discs flavored with saffron Net Wt: 12 Oz by BAPS Shayona. Reason: During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #5 & #6..
Details
Source
Food Recall
External ID
F-0491-2024
Action Date
2023-12-13
Status
Ongoing
Category
food
Product Description
BAPS SHAYONA Kesar Penda Ricotta fudge discs flavored with saffron Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53150 Contains: Milk
Lot/Code Info: 11G1323 BEST BY 9/11/2023, 04G0523 BEST BY 9/3/2023, 04F1523 BEST BY 8/14/2023, 04F0723 BEST BY 8/6/2023 & 04F0723 BEST BY 8/6/2023
Quantity Affected: 873 units
Reason for Recall
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #5 & #6.
Distribution
Product was shipped to the following states: AL, FL, GA, NC, SC & TN
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-27
Company
Lilburn, GA
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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
BAPS Shayona has 13 FDA actions in our database, including 13 recalls.
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 (BAPS Shayona) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BAPS Shayona have FDA actions?
BAPS Shayona has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0491-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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