SupplierRadar

Sanpellegrino S.p.A.

FDA import alert and refusal historySan Pellegrino Terme, ItalyFEI 3003235155

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Sanpellegrino S.p.A..

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectSanpellegrino S.p.A added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Sanpellegrino S.p.A. (San Pellegrino Terme, Italy) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sanbitter red soda, published by FDA on July 15, 2013, and has 1 FDA import refusal recorded since October 2016.

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

Current status

Last import refusal
Bottled spring or mineral water · USUAL NAME
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Sanpellegrino S.p.A.

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

2024

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

2019

  1. Import refusal
    Refused, Bottled spring or mineral waterUSUAL NAMELABELINGEntry AZW-0141005-3
    Source

2017

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2013

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source
  2. Import alert listing
    Listed on Import Alert 45-02red listSanbitter Red Soda
    Source

Refusal charges, in plain English

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • USUAL NAME1 refused line

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

Questions about Sanpellegrino S.p.A.

Is Sanpellegrino S.p.A. on an FDA import alert?
Yes. As of October 26, 2026, Sanpellegrino S.p.A. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sanbitter red soda; FDA published the listing on July 15, 2013.
Has FDA refused shipments from Sanpellegrino S.p.A.?
Yes. FDA refused 1 shipment line from Sanpellegrino S.p.A. on December 19, 2019. The most recent, on December 19, 2019, was bottled spring or mineral water, charged as USUAL NAME (common or usual name missing).
Why did FDA refuse Sanpellegrino S.p.A.'s shipments?
The most frequent charges are LABELING (fair packaging and labeling act, 1 line) and USUAL NAME (common or usual name missing, 1 line).
When was Sanpellegrino S.p.A. last inspected by FDA?
FDA's most recent inspection of Sanpellegrino S.p.A. with a final classification is dated June 21, 2024 and was classified VAI (Voluntary Action Indicated).
What is Sanpellegrino S.p.A.'s FEI number?
Sanpellegrino S.p.A.'s FDA Establishment Identifier (FEI) is 3003235155.
Can shipments from Sanpellegrino S.p.A. still enter the U.S.?
Shipments of sanbitter red soda from Sanpellegrino S.p.A. can be detained without physical examination under Import Alert 45-02; 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).

Buying from Sanpellegrino S.p.A.?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Sanpellegrino S.p.A..

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectSanpellegrino S.p.A added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.