Great Value Fruit Cocktail in Fruit Juice from Concentrate NET WT 15 OZ (425g) DISTRIBUTED BY: Walmart Inc., Bentonvill
Summary
The FDA issued a Class II for Great Value Fruit Cocktail in Fruit Juice from Concentrate NET WT 15 OZ (425g) by Pacific Coast Producers. Reason: Potential contamination with elevated levels of lead..
Details
Source
Food Recall
External ID
H-0167-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Great Value Fruit Cocktail in Fruit Juice from Concentrate NET WT 15 OZ (425g) DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 UPC: 078742369570
Lot/Code Info: Lot: 6FCB 04 C2263 BEST IF USED BY: SEP 01 2027
Quantity Affected: 1,836 cases (24 units/case)
Reason for Recall
Potential contamination with elevated levels of lead.
Distribution
Domestic: AL, AZ, LA, NM, PA, WA, WY. Foreign: Not applicable.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-10-01
Company
Lodi, CA
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 82 food recalls issued in the same week, part of 117 food-related FDA actions this month.
Pacific Coast Producers 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 (Pacific Coast Producers) 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 Producers have FDA actions?
Pacific Coast Producers 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 "H-0167-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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