Item #96522, King Harvest Lemon Hummus, net wt. 10oz., UPC 025726 31001 1, perishable and refrigerated, packed in sealed
Summary
The FDA issued a Class II for Item #96522, King Harvest Lemon Hummus, net wt. 10oz., UPC 025726 31001 1, peris by Pacific Coast Fresh CO. Reason: Plastic fragments.
Details
Source
Food Recall
External ID
F-0596-2025
Action Date
2025-03-12
Status
Terminated
Category
food
Product Description
Item #96522, King Harvest Lemon Hummus, net wt. 10oz., UPC 025726 31001 1, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Lot/Code Info: Expiration Dates: 2/5/2025 2/9/2025 2/12/2025 2/16/2025 2/19/2025 2/23/2025
Quantity Affected: 2084 cups total
Reason for Recall
Plastic fragments
Distribution
Distributed in Idaho, Oregon, and Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-04
Company
Portland, OR
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 37 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Pacific Coast Fresh CO has 19 FDA actions in our database, including 19 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 (Pacific Coast Fresh CO) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pacific Coast Fresh CO have FDA actions?
Pacific Coast Fresh CO has 19 FDA actions in our database, including 19 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0596-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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