Biggar and Leith
FDA import alert and refusal historyPortlaoise, IrelandFEI 3023015153
Recorded by FDA as BIGGAR AND LEITH
As of October 27, 2026, Biggar and Leith is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 22, 2022, most often for processor not registered for canned or acidified foods (NEEDS FCE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Pepper sauce (hot, mild, etc.) · NEEDS FCE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Biggar and Leith
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
Questions about Biggar and Leith
- Is Biggar and Leith on an FDA import alert?
- No listing for Biggar and Leith appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Ireland page.
- Has FDA refused shipments from Biggar and Leith?
- Yes. FDA refused 1 shipment line from Biggar and Leith on November 22, 2022. The most recent, on November 22, 2022, was pepper sauce (hot, mild, etc.), charged as NEEDS FCE (processor not registered for canned or acidified foods).
- Why did FDA refuse Biggar and Leith's shipments?
- The most frequent charge is NEEDS FCE (processor not registered for canned or acidified foods, 1 line).
- What is Biggar and Leith's FEI number?
- Biggar and Leith's FDA Establishment Identifier (FEI) is 3023015153.
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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.