RecallHawk
Class II Recall

First & Ten, Hot Sauce, NET WT. 11.5 OZ (326g), UPC code 195893089628

First & Ten LLC

Summary

The FDA issued a Class II for First & Ten, Hot Sauce, NET WT. 11.5 OZ (326g), UPC code 195893089628 by First & Ten LLC. Reason: Undeclared Allergen: Milk. Product label declares butter but does not list milk..

Details

Source

Food Recall

External ID

F-1075-2022

Action Date

2022-06-01

Status

Terminated

Category

food

Product Description

First & Ten, Hot Sauce, NET WT. 11.5 OZ (326g), UPC code 195893089628

Lot/Code Info: Best by Date: 10/20/2023; 12/10/2023; and 02/18/2024

Quantity Affected: 1,140 Bottles

Reason for Recall

Undeclared Allergen: Milk. Product label declares butter but does not list milk.

Distribution

Domestic distribution only.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-05

Company

First & Ten LLC

Venice, FL

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

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

How often does First & Ten LLC have FDA actions?

This is the only FDA action we have on record for First & Ten LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1075-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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