Pita Jungle Cilantro Jalapeno Hummus & Pita Chips packaged as individual "snack pack" in 9.2oz plastic clamshell contain
Summary
The FDA issued a Class II for Pita Jungle Cilantro Jalapeno Hummus & Pita Chips packaged as individual "snack by SSP America PHX, LLC. Reason: Finished product label does not declare sesame which is an ingredient of hummus (tahini)..
Details
Source
Food Recall
External ID
F-1783-2024
Action Date
2024-09-11
Status
Terminated
Category
food
Product Description
Pita Jungle Cilantro Jalapeno Hummus & Pita Chips packaged as individual "snack pack" in 9.2oz plastic clamshell container.
Lot/Code Info: Product labels stating Enjoy By: 07/20/24, 07/21/24, and 07/22/24.
Quantity Affected: 16 individual units
Reason for Recall
Finished product label does not declare sesame which is an ingredient of hummus (tahini).
Distribution
AZ
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-19
Company
Phoenix, AZ
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 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
SSP America PHX, LLC has 6 FDA actions in our database, including 6 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 (SSP America PHX, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SSP America PHX, LLC have FDA actions?
SSP America PHX, LLC has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1783-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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