Ricocrem Cozzo
FDA import alert and refusal historyCarini, ItalyFEI 3010123910
As of October 26, 2026, Ricocrem Cozzo (Carini, Italy) is on the red list of FDA Import Alert 12-10 (Cheese: microbiological contamination) for cannoli cream, published by FDA on August 24, 2021, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 12-10 · red list
- Last import refusal
- Cheese, ricotta · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ricocrem Cozzo
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- LISTERIA1 refused line
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
- POISONOUS1 refused line
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
Questions about Ricocrem Cozzo
- Is Ricocrem Cozzo on an FDA import alert?
- Yes. As of October 26, 2026, Ricocrem Cozzo is on the red list of FDA Import Alert 12-10, “Cheese: microbiological contamination”, for cannoli cream; FDA published the listing on August 24, 2021.
- Has FDA refused shipments from Ricocrem Cozzo?
- Yes. FDA refused 2 shipment lines from Ricocrem Cozzo between August 18, 2021 and November 10, 2021. The most recent, on November 10, 2021, was cheese, ricotta, charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Ricocrem Cozzo's shipments?
- The most frequent charges are LISTERIA (listeria monocytogenes, 1 line) and POISONOUS (poisonous or deleterious substance, 1 line).
- What is Ricocrem Cozzo's FEI number?
- Ricocrem Cozzo's FDA Establishment Identifier (FEI) is 3010123910.
- Can shipments from Ricocrem Cozzo still enter the U.S.?
- Shipments of cannoli cream from Ricocrem Cozzo can be detained without physical examination under Import Alert 12-10; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.