CLASS I Food recall · Reported 22 Nov 2023 · FDA Enforcement Report

Mamey, Paradise Flavors Llc recalled

Paradise Flavors is recalling Mamey, Paradise Flavors Llc, distributed in Florida. The recall was initiated on 27 Sep 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNone

Quantity recalled80 units (pieces) from latest production

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-0440-2024
FDA event ID: 93169
Recalling firm: Paradise Flavors, Marathon, FL
Brand: Mamey
Classification: Class I
Status: Terminated
Recall initiated: 27 Sep 2023
FDA classified: 17 Nov 2023
Reported: 22 Nov 2023
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Allergens
Product category: Other

Timeline

27 Sep 2023	Recall initiated by company
17 Nov 2023	Classified by FDA	+51 days
22 Nov 2023	Published in enforcement report	+5 days

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

Reason for recall

Undeclared allergen: Milk.

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

MAMEY, PARADISE FLAVORS LLC, 4 oz. Packaged in plastic pouch. Frozen.

Where it was distributed

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

Florida

Questions about this recall

Is Mamey, Paradise Flavors Llc recalled?

Yes. Paradise Flavors recalled Mamey, Paradise Flavors Llc on 27 Sep 2023. The recall is Class I and its status is Terminated. Recall number F-0440-2024.

Why was it recalled?

Undeclared allergen: Milk.

Which lots are affected?

None

Where was it sold?

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

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Paradise Flavors

All 39

Reported	Class	Recall	Company	Reason	Where
22 Nov 2023Food	CLASS I	Dulce DE Leche, Ice-cream base, Natural flavor recalledDulce DE	Paradise Flavors	Undeclared Allergens	FL
22 Nov 2023Food	CLASS I	Bubblegum Gummybear, ice-cream base, artificial flavor recalledBubblegum Gummybear	Paradise Flavors	Undeclared Allergens	FL
22 Nov 2023Food	CLASS I	Guava Jelly, Ice-cream base, natural flavoring, artificial coloring recalledGuava	Paradise Flavors	Undeclared Allergens	FL
22 Nov 2023Food	CLASS I	Trail Mix/Frutas Secas, Ice-cream base, dried fruits recalledTrail Mix	Paradise Flavors	Undeclared Allergens	FL
22 Nov 2023Food	CLASS I	Ferrero Rocher, Ice-cream base, Hazelnut, Nutella, Penuts recalledFerrero Rocher	Paradise Flavors	Undeclared Allergens	FL

Other Other recalls

All 4,664

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Food	CLASS I	Alfalfa, Net Weight 50 lbs. bag, Product of USA, International recalledAlfalfa	International Sprout Holdings	Salmonella	17 states
16 Sep 2026Food	CLASS I	Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalledCrown	Euro Foods Group USA NJ	Foreign Material	4 states
9 Sep 2026Food	CLASS I	Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic recalledItem	Ron's Home Style Foods	Salmonella	AR, OK, TX
9 Sep 2026Food	CLASS I	Food to Live Organic SuperGrass Powder recalled by Lexunder	Lexunder	Salmonella	40 states
3 Sep 2026Food	ANNOUNCED	Epinephrine Injection, USP 30 mg/ (1 mg/mL) multi dose vial recalledAmerican Regent, Inc.	American Regent	Particulate Matter	Nationwide