Is Rapenor S.A. on an FDA import alert?

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

Has FDA refused shipments from Rapenor S.A.?

Yes. FDA refused 2 shipment lines from Rapenor S.A. on November 30, 2018. The most recent, on November 30, 2018, was sauces, n.e.c., charged as LIST INGRE (ingredients not listed).

Why did FDA refuse Rapenor S.A.'s shipments?

The most frequent charges are LIST INGRE (ingredients not listed, 2 lines) and NO PROCESS (no scheduled process filed, 2 lines).

When was Rapenor S.A. last inspected by FDA?

FDA's most recent inspection of Rapenor S.A. with a final classification is dated July 10, 2019 and was classified VAI (Voluntary Action Indicated).

What is Rapenor S.A.'s FEI number?

Rapenor S.A.'s FDA Establishment Identifier (FEI) is 3011286172.

Rapenor S.A.

FDA import alert and refusal historyMontevideo, UruguayFEI 3011286172

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As of October 26, 2026, Rapenor S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 30, 2018, most often for ingredients not listed (LIST INGRE).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Nov 30, 2018Sauces, n.e.c. · LIST INGRE
Last warning letter: None found
Last inspection: Jul 10, 2019Classified VAI (Voluntary Action Indicated)

Every FDA record for Rapenor S.A.

3 records, newest first. Each line links to the FDA page it came from.

2019

Jul 10, 2019Inspection
Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
Source

2018

Nov 30, 2018Import refusal
Refused, 2 lines in one entry: Sauces, n.e.c.LIST INGRENO PROCESSEntry ARE-4240297-9Show 2 linesHide lines
- Refused, Sauces, n.e.c.LIST INGRE NO PROCESSEntry ARE-4240297-9Source
- Refused, Sauces, n.e.c.LIST INGRE NO PROCESSEntry ARE-4240297-9Source
Source

Refusal charges, in plain English

LIST INGRE2 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
NO PROCESS2 refused lines
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 Rapenor S.A.

Is Rapenor S.A. on an FDA import alert?: No listing for Rapenor S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Uruguay page.
Has FDA refused shipments from Rapenor S.A.?: Yes. FDA refused 2 shipment lines from Rapenor S.A. on November 30, 2018. The most recent, on November 30, 2018, was sauces, n.e.c., charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Rapenor S.A.'s shipments?: The most frequent charges are LIST INGRE (ingredients not listed, 2 lines) and NO PROCESS (no scheduled process filed, 2 lines).
When was Rapenor S.A. last inspected by FDA?: FDA's most recent inspection of Rapenor S.A. with a final classification is dated July 10, 2019 and was classified VAI (Voluntary Action Indicated).
What is Rapenor S.A.'s FEI number?: Rapenor S.A.'s FDA Establishment Identifier (FEI) is 3011286172.

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