grupo penafiel

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

Refusal charges, in plain English

• POISONOUS4 refused lines

  Poisonous or deleterious substance

  The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

• FALSE1 refused line

  False or misleading labeling

  The labeling appeared to be false or misleading in some particular.

• JUICE %1 refused line

  Juice percentage not declared

  The product is presented as a beverage containing fruit or vegetable juice and the label appeared not to state the total percentage of juice on the information panel.

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about grupo penafiel

Is grupo penafiel on an FDA import alert?

Yes. As of October 26, 2026, grupo penafiel is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for carbonated water; FDA published the listing on March 3, 2022.

Has FDA refused shipments from grupo penafiel?

Yes. FDA refused 5 shipment lines from grupo penafiel between May 7, 2018 and August 22, 2024. The most recent, on August 22, 2024, was carbonated water (nonmedicinal), n.e.c., charged as POISONOUS (poisonous or deleterious substance).

Why did FDA refuse grupo penafiel's shipments?

The most frequent charges are POISONOUS (poisonous or deleterious substance, 4 lines) and FALSE (false or misleading labeling, 1 line).

What is grupo penafiel's FEI number?

grupo penafiel's FDA Establishment Identifier (FEI) is 3010965131.

Can shipments from grupo penafiel still enter the U.S.?

Shipments of carbonated water from grupo penafiel can be detained without physical examination under Import Alert 99-42; 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).