The Tomato Head Beet Hummus packaged in 8oz PPE plastic cups - 8 cups per case
Summary
The FDA issued a Class II for The Tomato Head Beet Hummus packaged in 8oz PPE plastic cups - 8 cups per case by Tomato Head Foods. Reason: Potential Metal Fragments within product.
Details
Source
Food Recall
External ID
F-0167-2023
Action Date
2022-11-30
Status
Terminated
Category
food
Product Description
The Tomato Head Beet Hummus packaged in 8oz PPE plastic cups - 8 cups per case
Lot/Code Info: Batch/Lot No. 010823 Product No. 0854259008061 Best By 01/08/23
Quantity Affected: 72 cases
Reason for Recall
Potential Metal Fragments within product
Distribution
Distributed to DCs located in: CA, FL, GA, IL
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-04
Company
Knoxville, TN
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 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tomato Head Foods has 2 FDA actions in our database, including 2 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 (Tomato Head Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tomato Head Foods have FDA actions?
Tomato Head Foods 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-0167-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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