Materne - Confilux

2 records, 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.

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Materne - Confilux

Is Materne - Confilux on an FDA import alert?

No listing for Materne - Confilux appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Belgium page.

Has FDA refused shipments from Materne - Confilux?

Yes. FDA refused 1 shipment line from Materne - Confilux on August 23, 2024. The most recent, on August 23, 2024, was other fruits, mixed, flavored jams, jellies, preserves, marmalades, butters and candied, charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse Materne - Confilux's shipments?

The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 1 line) and NO PROCESS (no scheduled process filed, 1 line).

When was Materne - Confilux last inspected by FDA?

FDA's most recent inspection of Materne - Confilux with a final classification is dated March 22, 2013 and was classified NAI (No Action Indicated).

What is Materne - Confilux's FEI number?

Materne - Confilux's FDA Establishment Identifier (FEI) is 3002824770.