RecallHawk
Class I Recall

Mixed Fruit: Mixed Fruit Burst 6/10 oz. UPC: 840219168357 Packaged in clamshell containers Mixed Fruit Chunk 4/32 oz. U

TGD Cuts, LLC

Summary

The FDA issued a Class I for Mixed Fruit: Mixed Fruit Burst 6/10 oz. UPC: 840219168357 Packaged in clamshell by TGD Cuts, LLC. Reason: Potential Salmonella Contamination.

Details

Source

Food Recall

External ID

F-0682-2024

Action Date

2023-12-27

Status

Terminated

Category

food

Product Description

Mixed Fruit: Mixed Fruit Burst 6/10 oz. UPC: 840219168357 Packaged in clamshell containers Mixed Fruit Chunk 4/32 oz. UPC: 840219109947 Packaged in clamshell containers Mixed Fruit Chunk 4/6 oz. UPC: 840219198606 Packaged in clamshell containers Mixed Fruit Chunks 1" 20 lb. UPC: 840219178912 Packaged in buckets Mixed Fruit Chunks 6/16 oz. UPC: 840219170480 Packaged in clamshell containers Mixed Fruit Chunks 3/30 oz. UPC: 840219165219 Packaged in clamshell containers Mixed Fruit Chunks 6/9 oz. UPC: 840219165196 Packaged in clamshell containers

Lot/Code Info: Use by start dates:11/23/2023, 11/3/2023, 23297, 11/2/2023 Use by end dates: 11/23/2023, 11/24/2023, 23317

Quantity Affected: 1223 units

Reason for Recall

Potential Salmonella Contamination

Distribution

Distributed in PA, NJ, MD, WV, SC VA, DE, NC, and NY

Type: Voluntary: Firm initiated

Recall Initiated: 2023-11-29

Company

TGD Cuts, LLC

Jessup, MD

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 157 food recalls issued in the same week, part of 204 food-related FDA actions this month.

TGD Cuts, LLC has 23 FDA actions in our database, including 23 recalls.

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 (TGD Cuts, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does TGD Cuts, LLC have FDA actions?

TGD Cuts, LLC has 23 FDA actions in our database, including 23 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0682-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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