RecallHawk
Class I Recall

Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [20 oz. (1 lb. 4 oz) 567g] with UPC# 7 965

Ray & Mascari,Inc

Summary

The FDA issued a Class I for Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [2 by Ray & Mascari,Inc. Reason: Potential Contamination of Salmonella..

Details

Source

Food Recall

External ID

F-0776-2025

Action Date

2025-05-21

Status

Terminated

Category

food

Product Description

Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [20 oz. (1 lb. 4 oz) 567g] with UPC# 7 96553 20062 1; 12 retail clam shells per case. Bulk 25# 6x6 tomatoes (cardboard case), bulk 10# 6x6 Tomatoes (cardboard case), bulk 25# Random #2 Tomatoes (cardboard case), bulk 20# 5x6 Vine Ripe (cardboard case).

Lot/Code Info: Lot Numbers: RM 250420 15250A RM 250421 15250A RM 250422 15250A RM 250424 15250B RM 250425 15250B RM 250427 15250B

Quantity Affected: 510 cases

Reason for Recall

Potential Contamination of Salmonella.

Distribution

IN KY MA MD MI NC OH PA WI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-04-30

Company

Ray & Mascari,Inc

Indianapolis, IN

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

How often does Ray & Mascari,Inc have FDA actions?

This is the only FDA action we have on record for Ray & Mascari,Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0776-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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