RecallHawk
Class I Recall

SAVPAK Duro 10x10, 8oz plastic bag, DISTRIBUTED BY: Southcoast Product Inc. Dallas, Texas 75215; UPC 29661 00076.

Rancho Santo Cristo, Inc

Summary

The FDA issued a Class I for SAVPAK Duro 10x10, 8oz plastic bag, DISTRIBUTED BY: Southcoast Product Inc. Dall by Rancho Santo Cristo, Inc. Reason: Undeclared Wheat Allergen.

Details

Source

Food Recall

External ID

F-1646-2024

Action Date

2024-08-14

Status

Terminated

Category

food

Product Description

SAVPAK Duro 10x10, 8oz plastic bag, DISTRIBUTED BY: Southcoast Product Inc. Dallas, Texas 75215; UPC 29661 00076.

Lot/Code Info: P63470, P63510, P64293

Quantity Affected: 246 units

Reason for Recall

Undeclared Wheat Allergen

Distribution

Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2024-06-12

Company

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

Rancho Santo Cristo, Inc 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 (Rancho Santo Cristo, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Rancho Santo Cristo, Inc have FDA actions?

Rancho Santo Cristo, Inc 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-1646-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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