RecallHawk
Class II Recall

BAPS SHAYONA Kaju Pista Roll Sweet rolls made from cashew and pistachio filling Net Wt: 12 Oz 460 Rockbridge Rd NW Lilbu

BAPS Shayona

Summary

The FDA issued a Class II for BAPS SHAYONA Kaju Pista Roll Sweet rolls made from cashew and pistachio filling by BAPS Shayona. Reason: During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6 and Blue 1..

Details

Source

Food Recall

External ID

F-0490-2024

Action Date

2023-12-13

Status

Ongoing

Category

food

Product Description

BAPS SHAYONA Kaju Pista Roll Sweet rolls made from cashew and pistachio filling Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53068 Contains: Nuts

Lot/Code Info: 02F1823 BEST BY 8/2/23

Quantity Affected: 138 units

Reason for Recall

During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6 and Blue 1.

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-0490-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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