RecallHawk
Class II Recall

BAPS SHAYONA Kaju Katri Kesar Cashew fudge flavored with saffron Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UP

BAPS Shayona

Summary

The FDA issued a Class II for BAPS SHAYONA Kaju Katri Kesar Cashew fudge flavored with saffron Net Wt: 12 Oz 4 by BAPS Shayona. Reason: During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5..

Details

Source

Food Recall

External ID

F-0489-2024

Action Date

2023-12-13

Status

Ongoing

Category

food

Product Description

BAPS SHAYONA Kaju Katri Kesar Cashew fudge flavored with saffron Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53065 Contains: Nut

Lot/Code Info: 10G1323 BEST BY 08/26/23

Quantity Affected: 296 units

Reason for Recall

During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5.

Distribution

Product was shipped to the following states: AL, FL, GA, NC, SC & TN

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-27

Company

BAPS Shayona

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-0489-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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