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Happy Mama Srl

FDA import alert and refusal historyCavriago, ItalyFEI 3011846987

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Example subjectHappy Mama Sr added to Import Alert 16-129 (red list)

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As of October 26, 2026, Happy Mama Srl is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 1, 2025, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Vegetable (single ingredient not mentioned elsewhere) soup · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Happy Mama Srl

1 record, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, Vegetable (single ingredient not mentioned elsewhere) soupNO PROCESSEntry 9RN-1214496-7
    Source

Refusal charges, in plain English

  • 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 Happy Mama Srl

Is Happy Mama Srl on an FDA import alert?
No listing for Happy Mama Srl appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Italy page.
Has FDA refused shipments from Happy Mama Srl?
Yes. FDA refused 1 shipment line from Happy Mama Srl on July 1, 2025. The most recent, on July 1, 2025, was vegetable (single ingredient not mentioned elsewhere) soup, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Happy Mama Srl's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
What is Happy Mama Srl's FEI number?
Happy Mama Srl's FDA Establishment Identifier (FEI) is 3011846987.

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Example subjectHappy Mama Sr 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.