Hollandia Dairy, Inc. 100% Appleberry Juice; Half Pint (236mL). UPC: 0 27495 03679 6
Summary
The FDA issued a Class II for Hollandia Dairy, Inc. 100% Appleberry Juice; Half Pint (236mL). UPC: 0 27495 036 by Hollandia Dairy, Inc.. Reason: 100% Appleberry Juice contaminated with cleaning solution, Peracetic Acid..
Details
Source
Food Recall
External ID
H-0307-2026
Action Date
2025-12-24
Status
Terminated
Category
food
Product Description
Hollandia Dairy, Inc. 100% Appleberry Juice; Half Pint (236mL). UPC: 0 27495 03679 6
Lot/Code Info: Nov 28
Quantity Affected: 22,700 units
Reason for Recall
100% Appleberry Juice contaminated with cleaning solution, Peracetic Acid.
Distribution
Various schools in San Bernardino, Highland, Romoland, Menifee, Winchester, Hemet, Fontana, and Camp Pendleton.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-05
Company
San Marcos, 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 87 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Hollandia Dairy, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hollandia Dairy, Inc. have FDA actions?
This is the only FDA action we have on record for Hollandia Dairy, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0307-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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