Andronico's COMMUNITY MARKETS 100% SQUEEZED ORANGE ANDROINCO'S COMMUNITY MARKETS SAN LEANDRO, CA 94577 16 OZ: UPC 675
Summary
The FDA issued a Class II for Andronico's COMMUNITY MARKETS 100% SQUEEZED ORANGE ANDROINCO'S COMMUNITY MARKE by Voila Juice Company. Reason: Product not processed to achieve 5-log pathogen reduction..
Details
Source
Food Recall
External ID
H-0166-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Andronico's COMMUNITY MARKETS 100% SQUEEZED ORANGE ANDROINCO'S COMMUNITY MARKETS SAN LEANDRO, CA 94577 16 OZ: UPC 675643050967 32 OZ: UPC 675643050974 64 OZ: UPC 675643050981
Lot/Code Info: Exp: 10/14/26
Quantity Affected: 32 gallons (total)
Reason for Recall
Product not processed to achieve 5-log pathogen reduction.
Distribution
Domestic: CA. Foreign: Not applicable.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-10-02
Company
Oakland, 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.
Voila Juice Company has 2 FDA actions in our database, including 2 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 (Voila Juice Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Voila Juice Company have FDA actions?
Voila Juice Company has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0166-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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