RecallHawk
Class II Recall

Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer

FACTOR

Summary

The FDA issued a Class II for Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single s by FACTOR. Reason: Undeclared Milk Allergen.

Details

Source

Food Recall

External ID

F-0829-2022

Action Date

2022-03-16

Status

Terminated

Category

food

Product Description

Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer

Lot/Code Info: Best By: 03/02/2022 Lot Number: 03/02/2022

Quantity Affected: 21,725 trays

Reason for Recall

Undeclared Milk Allergen

Distribution

AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY

Type: Voluntary: Firm initiated

Recall Initiated: 2022-02-23

Company

FACTOR

Aurora, IL

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

FACTOR has 7 FDA actions in our database, including 7 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 (FACTOR) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does FACTOR have FDA actions?

FACTOR has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0829-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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