RecallHawk
Class III Recall

Gelato ice cream packaged in Compostable Tubs which are labeled in part Vaschetta Accoppiata Compostabile . The gelato

ALCAS USA CORP.

Summary

The FDA issued a Class III for Gelato ice cream packaged in Compostable Tubs which are labeled in part Vaschet by ALCAS USA CORP.. Reason: Possible Fragmentation of Ice Cream Tub (Container) Made of Compostable Material..

Details

Source

Food Recall

External ID

F-0024-2025

Action Date

2024-10-16

Status

Terminated

Category

food

Product Description

Gelato ice cream packaged in Compostable Tubs which are labeled in part Vaschetta Accoppiata Compostabile . The gelato is packaged in four (4) sizes of Compostable Tubs: COMPOSTABLE YETI TUB 350 GR/ 500 CC (M) (16.90 fl. oz.) COMPOSTABLE YETI TUB 500 Gr/750 CC (25.36 fl. oz.) (L) COMPOSTABLE YETI TUB 750 Gr/1000 CC (33.81 fl. oz.) (XL) COMPOSTABLE YETI TUB 1000 Gr/1500 CC (50.72 fl. oz.) (XXL)

Lot/Code Info: 305002070 YETI BIO GR350/CC450 305002080 YETI BIO GR500/CC650 305002090 YETI BIO GR750/CC900 305002100 YETI BIO GR1000/CC1250

Quantity Affected: Total 834 COMPOSTABLE YETI TUBS

Reason for Recall

Possible Fragmentation of Ice Cream Tub (Container) Made of Compostable Material.

Distribution

USA, Cayman Islands and Canada

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-15

Company

ALCAS USA CORP.

Fort Lauderdale, FL

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 25 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (ALCAS USA CORP.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does ALCAS USA CORP. have FDA actions?

This is the only FDA action we have on record for ALCAS USA CORP. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0024-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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