Pelican Canning Co
FDA import alert and refusal historySfagia, GreeceFEI 10020
As of October 26, 2026, Pelican Canning Co (Sfagia, Greece) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for great northern beans; great northern bean; elephant beans in tomato sauce; great northern beans packed in tomato sauce with soya bean oil, 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 99-37 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pelican Canning Co
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-37red listGreat northern beans; great northern bean; elephant beans in tomato sauce; great northern beans packed in tomato sauce with soya bean oilSource
Questions about Pelican Canning Co
- Is Pelican Canning Co on an FDA import alert?
- Yes. As of October 26, 2026, Pelican Canning Co is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for great northern beans; great northern bean; elephant beans in tomato sauce; great northern beans packed in tomato sauce with soya bean oil; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Pelican Canning Co?
- No FDA import refusals for Pelican Canning Co appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Pelican Canning Co's FEI number?
- Pelican Canning Co's FDA Establishment Identifier (FEI) is 10020.
- Can shipments from Pelican Canning Co still enter the U.S.?
- Shipments of great northern beans; great northern bean; elephant beans in tomato sauce; great northern beans packed in tomato sauce with soya bean oil from Pelican Canning Co can be detained without physical examination under Import Alert 99-37; 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.