RecallHawk
Class I Recall

Golden Owl Dried Mango 7 oz (200g) UPC 816710-024461. Packaged in clear non-flex plastic jars. 24 jars per case.

TRUONG GIANG WAREHOUSE

Summary

The FDA issued a Class I for Golden Owl Dried Mango 7 oz (200g) UPC 816710-024461. Packaged in clear non-flex by TRUONG GIANG WAREHOUSE. Reason: Undeclared sulfites.

Details

Source

Food Recall

External ID

F-1024-2024

Action Date

2024-03-13

Status

Terminated

Category

food

Product Description

Golden Owl Dried Mango 7 oz (200g) UPC 816710-024461. Packaged in clear non-flex plastic jars. 24 jars per case.

Quantity Affected: 98 cases

Reason for Recall

Undeclared sulfites

Distribution

Distributed to FL, GA, IL, MA, MI, MN, MO, NC, NE, NY, OH, PA, RI, SC, TN, VA, and WI.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-23

Company

TRUONG GIANG WAREHOUSE

Philadelphia, PA

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 124 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 (TRUONG GIANG WAREHOUSE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does TRUONG GIANG WAREHOUSE have FDA actions?

This is the only FDA action we have on record for TRUONG GIANG WAREHOUSE in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1024-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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