RecallHawk
Class II Recall

1/2" Diced Tomatoes in Juice packed in 55 gallon fiber drums

Ingomar Packing Co

Summary

The FDA issued a Class II for 1/2" Diced Tomatoes in Juice packed in 55 gallon fiber drums by Ingomar Packing Co. Reason: Foreign object; plastic.

Details

Source

Food Recall

External ID

F-0708-2024

Action Date

2024-01-17

Status

Terminated

Category

food

Product Description

1/2" Diced Tomatoes in Juice packed in 55 gallon fiber drums

Lot/Code Info: Product code 9555105DI- lot codes: too numerous to list- please see Attachment B

Quantity Affected: 4,038 drums

Reason for Recall

Foreign object; plastic

Distribution

U.S. Distribution to CA and WA. Foreign distribution to Japan.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-03

Company

Ingomar Packing Co

Los Banos, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 26 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Ingomar Packing Co has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Ingomar Packing Co) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ingomar Packing Co have FDA actions?

Ingomar Packing Co 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-0708-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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