De Langlade & Grancelli
FDA import alert and refusal historyGenoa, ItalyFEI 11080
As of October 25, 2026, De Langlade & Grancelli (Genoa, Italy) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for pesto alla genovese (genoese greensauce) (basil; cheese; olive oil; garlic); tuna in olive oil; baby clams in brine, published by FDA on June 3, 2014, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-36 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for De Langlade & Grancelli
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listPesto alla genovese (genoese greensauce) (basil; cheese; olive oil; garlic); tuna in olive oil; baby clams in brineSource
Questions about De Langlade & Grancelli
- Is De Langlade & Grancelli on an FDA import alert?
- Yes. As of October 25, 2026, De Langlade & Grancelli is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for pesto alla genovese (genoese greensauce) (basil; cheese; olive oil; garlic); tuna in olive oil; baby clams in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from De Langlade & Grancelli?
- No FDA import refusals for De Langlade & Grancelli appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is De Langlade & Grancelli's FEI number?
- De Langlade & Grancelli's FDA Establishment Identifier (FEI) is 11080.
- Can shipments from De Langlade & Grancelli still enter the U.S.?
- Shipments of pesto alla genovese (genoese greensauce) (basil; cheese; olive oil; garlic); tuna in olive oil; baby clams in brine from De Langlade & Grancelli can be detained without physical examination under Import Alert 99-36; 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.