Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packaged in round plastic clear container, net wt. 8oz. There are 1
Summary
The FDA issued a Class I for Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packaged in round plastic cl by Lydia Pack 3 Inc. Reason: Hummus product label declares Tahini but does not declare sesame..
Details
Source
Food Recall
External ID
F-0867-2024
Action Date
2024-02-21
Status
Terminated
Category
food
Product Description
Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12341 4. The recalled product label declares: Ingredients: Garbanzo Beans, Tahini Paste, Garlico (Fresh Garlic/Oil/Lemon/Salt), Natural Citric Acid, Salt.
Lot/Code Info: All dates up to and includes 1/25/2024
Quantity Affected: 3,000 to 4,000 packages
Reason for Recall
Hummus product label declares Tahini but does not declare sesame.
Distribution
Distributed in OR and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-01-19
Company
Milwaukie, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lydia Pack 3 Inc has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Lydia Pack 3 Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lydia Pack 3 Inc have FDA actions?
Lydia Pack 3 Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0867-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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