ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contains: Sugar, Water, Citric Acid Natural Fla
Summary
The FDA issued a Class II for ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contain by A C Calderoni & Co. Inc.. Reason: Potential contamination with yeast (yeast growth in product).
Details
Source
Food Recall
External ID
F-0643-2025
Action Date
2025-03-12
Status
Terminated
Category
food
Product Description
ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contains: Sugar, Water, Citric Acid Natural Flavor, Sodium Benzoate; Refrigerate after opening
Lot/Code Info: ACC22224
Quantity Affected: 68 cases (12 bottles/case)
Reason for Recall
Potential contamination with yeast (yeast growth in product)
Distribution
To one direct consignee, located in California, who further distributed to foodservice distributors and restaurants.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-15
Company
Brisbane, 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 37 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 (A C Calderoni & Co. Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does A C Calderoni & Co. Inc. have FDA actions?
This is the only FDA action we have on record for A C Calderoni & Co. Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0643-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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