King Harvest Spinach Hummus, perishable and refrigerated, packed in plastic tubs with tamper evident lids. Net wt. 10oz.
Summary
The FDA issued a Class II for King Harvest Spinach Hummus, perishable and refrigerated, packed in plastic tubs by Pacific Coast Fresh CO. Reason: Recall initiated due to potential plastic fragments..
Details
Source
Food Recall
External ID
F-0031-2025
Action Date
2024-10-23
Status
Terminated
Category
food
Product Description
King Harvest Spinach Hummus, perishable and refrigerated, packed in plastic tubs with tamper evident lids. Net wt. 10oz. Dist. Exclusively by Pacific Coast Fresh Co Portland, Oregon. UPC 0 25726 31108 7.
Lot/Code Info: Use by 10/08/24
Quantity Affected: 994 tubs
Reason for Recall
Recall initiated due to potential plastic fragments.
Distribution
Distributed in OR and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-28
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 33 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-0031-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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