RecallHawk
Class I Recall

ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case

Muktanand Foods Inc

Summary

The FDA issued a Class I for ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear by Muktanand Foods Inc. Reason: Undeclared sulfites.

Details

Source

Food Recall

External ID

F-1748-2022

Action Date

2022-09-28

Status

Terminated

Category

food

Product Description

ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case

Lot/Code Info: All product regardless of the presence or absence of a batch number on the product

Quantity Affected: 485 cases

Reason for Recall

Undeclared sulfites

Distribution

AL CO GA IA IL KS MN MO NC NE NJ OH SC WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-08

Company

Muktanand Foods Inc

Bensenville, IL

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Muktanand Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Muktanand Foods Inc have FDA actions?

This is the only FDA action we have on record for Muktanand Foods Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1748-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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