Class IITerminatedVoluntary: Firm initiated

A C Calderoni & Co. Inc.: food recall F-0643-2025

A C Calderoni & Co. Inc. of Brisbane, CA recalled ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contains: Sugar, Water, Citric Acid Natural… Reason: Potential contamination with yeast (yeast growth in product). The FDA listed it as Class II in its Enforcement Report dated Mar 12, 2025; distribution: California.

Record status as published: Terminated (terminated Apr 23, 2025). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
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
Product quantity
68 cases (12 bottles/case)
Reason for recall
Potential contamination with yeast (yeast growth in product)
Codes, lots and dates on the package
ACC22224
Distribution pattern
To one direct consignee, located in California, who further distributed to foodservice distributors and restaurants.
Recalling firm
A C Calderoni & Co. Inc., Brisbane, CA
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Other

Dates

EventDate
Recall initiated by the firmNov 15, 2022
Classified by the FDAMar 19, 2025
Published in the Enforcement ReportMar 12, 2025
TerminatedApr 23, 2025

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0643-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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