CLASS II Food recall · Reported 12 Jun 2024 · FDA Enforcement Report

Pink Lemonde recalled by Charles Boggini Company

Charles Boggini Company is recalling Pink Lemonde, distributed in 9 states. The recall was initiated on 29 Mar 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot/Unit Numnber: 1-017
Quantity recalled28 gallons

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-1284-2024
FDA event ID
94334
Recalling firm
Charles Boggini Company, Coventry, CT
Classification
Class II
Status
Terminated
Recall initiated
29 Mar 2024
FDA classified
3 Jun 2024
Reported
12 Jun 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Citrus

Timeline

29 Mar 2024Recall initiated by company
3 Jun 2024Classified by FDA+66 days
12 Jun 2024Published in enforcement report+9 days

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

Reason for recall

Products contain undeclared FD&C Red No. 40

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Charles Boggini Pink Lemonde; 1 or 5 U.S. Gallons

Where it was distributed

CT, PA, NY, NJ, AZ, MI, IL, NV, CA

ArizonaCaliforniaConnecticutIllinoisMichiganNew JerseyNevadaNew YorkPennsylvania

Questions about this recall

Why was it recalled?

Products contain undeclared FD&C Red No. 40

Which lots are affected?

Lot/Unit Numnber: 1-017

Where was it sold?

CT, PA, NY, NJ, AZ, MI, IL, NV, CA

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.

Other products in this recall event

2 other products · FDA event 94334

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