Recall record at a glance
| Official record | F-0024-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | ALCAS USA CORP. |
| Report date | Oct 16, 2024 |
| Recall initiation date | May 15, 2024 |
| Quantity | Total 834 COMPOSTABLE YETI TUBS |
| Location | Fort Lauderdale, FL, United States |
Official 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)
Why the product was recalled
Possible Fragmentation of Ice Cream Tub (Container) Made of Compostable Material.
Distribution information
USA, Cayman Islands and Canada
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.