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Refrescos India Quiche

FDA import alert and refusal historySta Cruz del Quiche, GuatemalaFEI 2000022602

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Example subjectRefrescos India Quich added to Import Alert 16-129 (red list)

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As of October 26, 2026, Refrescos India Quiche is not on any FDA import alert in SupplierRadar's records; FDA refused 13 of its shipment lines between February 4, 2021 and September 18, 2025, most often for ingredients not listed (LIST INGRE).

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

Current status

Import alerts
Not listed
Last import refusal
Soft drink, citrus fruit flavored, carbonated · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Refrescos India Quiche

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

2025

  1. Import refusal
    Refused, 2 lines in one entry: Soft drink, citrus fruit flavored, carbonatedLIST INGRELACKS N/CNO ENGLISHNUTRIT LBLEntry HG8-1601611-4Show 2 lines
    Source

2023

  1. Import refusal
    Refused, 4 lines in one entry: Carbonated soft drink, n.e.c.; Soft drink, citrus fruit flavored, carbonated and 1 moreLIST INGRELACKS N/CNO ENGLISHNUTRIT LBLEntry DM4-0639235-5Show 4 lines
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Carbonated soft drink, n.e.c.LIST INGRELACKS N/CNO ENGLISHNUTRIT LBLEntry DM4-0640906-8Show 2 lines
    Source

2021

  1. Import refusal
    Refused, 2 lines in one entry: Soft drink, subtropical or tropical fruit flavored, carbonatedLIST INGRELACKS N/CNO ENGLISHNUTRIT LBLEntry DM4-0579988-1Show 2 lines
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Soft drink, citrus fruit flavored, carbonatedLIST INGRENO ENGLISHNUTRIT LBLEntry E84-0097936-3Show 2 lines
    Source
  3. Import refusal
    Refused, Soft drink, subtropical or tropical fruit flavored, carbonatedLIST INGRENO ENGLISHLABELINGNUTRIT LBLEntry E84-0096919-0
    Source

Refusal charges, in plain English

  • LIST INGRE13 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 ENGLISH13 refused lines

    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 LBL13 refused lines

    Nutrition information missing from label

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

  • LACKS N/C10 refused lines

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • 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.

Questions about Refrescos India Quiche

Is Refrescos India Quiche on an FDA import alert?
No listing for Refrescos India Quiche appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
Has FDA refused shipments from Refrescos India Quiche?
Yes. FDA refused 13 shipment lines from Refrescos India Quiche between February 4, 2021 and September 18, 2025. The most recent, on September 18, 2025, was soft drink, citrus fruit flavored, carbonated, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Refrescos India Quiche's shipments?
The most frequent charges are LIST INGRE (ingredients not listed, 13 lines) and NO ENGLISH (required label information not in english, 13 lines).
What is Refrescos India Quiche's FEI number?
Refrescos India Quiche's FDA Establishment Identifier (FEI) is 2000022602.

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Example subjectRefrescos India Quich added to Import Alert 16-129 (red list)

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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.