CLASS II Food recall · Reported 12 Mar 2025 · FDA Enforcement Report

Orgeat Almond Syrup;; with screw-top lid recalled by A C Calderoni & Co

A C Calderoni & Co is recalling Orgeat Almond Syrup;; with screw-top lid, distributed in California. The recall was initiated on 15 Nov 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesACC22224
Quantity recalled68 cases (12 bottles/case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0643-2025
FDA event ID
96265
Recalling firm
A C Calderoni & Co, Brisbane, CA
Brand
Orgeat
Classification
Class II
Status
Terminated
Recall initiated
15 Nov 2022
FDA classified
19 Mar 2025
Reported
12 Mar 2025
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Mold
Product category
Nuts

Timeline

15 Nov 2022Recall initiated by company
12 Mar 2025Published in enforcement report+848 days
19 Mar 2025Classified by FDA+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential contamination with yeast (yeast growth in product)

Product as listed by the FDA

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

Where it was distributed

To one direct consignee, located in California, who further distributed to foodservice distributors and restaurants.

California

Questions about this recall

Why was it recalled?

Potential contamination with yeast (yeast growth in product)

Which lots are affected?

ACC22224

Where was it sold?

To one direct consignee, located in California, who further distributed to foodservice distributors and restaurants.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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