Thick-It Original Food & Beverage Thickener 6/36 oz. jars per case
Summary
The FDA issued a Class III for Thick-It Original Food & Beverage Thickener 6/36 oz. jars per case by Kent Precision Foods Group, Inc.. Reason: Food and beverage thickener recalled because of possible insanitary conditions during manufacturing.
Details
Source
Food Recall
External ID
F-1688-2022
Action Date
2022-09-14
Status
Terminated
Category
food
Product Description
Thick-It Original Food & Beverage Thickener 6/36 oz. jars per case
Lot/Code Info: 2B0045802 best by 10/2024 2B0042678 best by 11/2024
Quantity Affected: 14 cases
Reason for Recall
Food and beverage thickener recalled because of possible insanitary conditions during manufacturing
Distribution
Distributed to food service distributors for use in hospitals, nursing homes and similar facilities. Specific distribution information pending.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-09
Company
Muscatine, IA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 129 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kent Precision Foods Group, Inc. has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Kent Precision Foods Group, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kent Precision Foods Group, Inc. have FDA actions?
Kent Precision Foods Group, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1688-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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