RecallHawk
Class I Recall

Terrafina Golden Raisins Net Wt. 10oz (283g) UPC:847938001385. Packaged in a plastic container, 8 containers per case.

SUNCO & FRENCHIE LLC.

Summary

The FDA issued a Class I for Terrafina Golden Raisins Net Wt. 10oz (283g) UPC:847938001385. Packaged in a pla by SUNCO & FRENCHIE LLC.. Reason: Undeclared sulfites.

Details

Source

Food Recall

External ID

F-1794-2024

Action Date

2024-09-11

Status

Terminated

Category

food

Product Description

Terrafina Golden Raisins Net Wt. 10oz (283g) UPC:847938001385. Packaged in a plastic container, 8 containers per case.

Lot/Code Info: Best If Used By 08/2025, Lot#GRA240602 Best If Used By 05/2025, Lot# GDR240901

Quantity Affected: 1280 lbs

Reason for Recall

Undeclared sulfites

Distribution

Distributed to distributor in NY and then further distributed to retailers in NY.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-08-22

Company

SUNCO & FRENCHIE LLC.

Pine Brook, NJ

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

SUNCO & FRENCHIE LLC. has 2 FDA actions in our database, including 2 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 (SUNCO & FRENCHIE LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does SUNCO & FRENCHIE LLC. have FDA actions?

SUNCO & FRENCHIE LLC. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1794-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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