RecallHawk
Class II Recall

ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contains: Sugar, Water, Citric Acid Natural Fla

A C Calderoni & Co. Inc.

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

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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