Factor Summertime Filet & Sweet Corn Risotto with Sweet Peach-Berry Crumble & Zucchini Medley 15.2oz.
Summary
The FDA issued a Class II for Factor Summertime Filet & Sweet Corn Risotto with Sweet Peach-Berry Crumble & Zu by FACTOR. Reason: Products contain an arborio rice ingredient that was recalled by the supplier because it contains glass.
Details
Source
Food Recall
External ID
F-1549-2022
Action Date
2022-08-24
Status
Terminated
Category
food
Product Description
Factor Summertime Filet & Sweet Corn Risotto with Sweet Peach-Berry Crumble & Zucchini Medley 15.2oz.
Lot/Code Info: best by 07/20/2022
Quantity Affected: 10545 units
Reason for Recall
Products contain an arborio rice ingredient that was recalled by the supplier because it contains glass
Distribution
Unknown, recalling company refused to provide distribution information
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-14
Company
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 38 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-1549-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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