Paradise Flavors LLC Recall: Undeclared allergen: Milk. Undeclared color additives: FD&C red #40, red #6, red #5, blue #1, and yellow #5.

🇺🇸 United States

1. September 27, 2023 - Recall initiated
2. November 22, 2023 - Reported by source
3. January 25, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0442-2024

Event ID

93169

Status

Terminated

Classification

Class I

Company

Paradise Flavors LLC

Product description

FLORIDA SUNRISE/CHEMIS, Paradise Flavors LLC, Ice-cream base, natural flavoring, artificial flavor and color., DISTRIBUTED BY PARADISE FLAVORS LLC, 3 oz, 120 ML. Packaged in plastic pouch. Frozen.

Quantity

108 units (pieces) from latest production

Reason

Undeclared allergen: Milk. Undeclared color additives: FD&C red #40, red #6, red #5, blue #1, and yellow #5.

Recall initiation date

September 27, 2023

Report date

November 22, 2023

Classification date

Not published in this source record

Termination date

January 25, 2024

Distribution pattern

Domestic distribution only, within state of Florida. No foreign distribution.

UPC, lot, and code information

None

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 93169 with 10 other product entries in Public Health Trace.

Responsible company: Paradise Flavors LLC

Other recalls from Paradise Flavors LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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