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Gruvipa S.L.

FDA import alert and refusal historyPineda De Mar, SpainFEI 3014321363

Recorded by FDA as GRUVIPA S.L.

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Example subjectGruvipa S.L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gruvipa S.L. has no FDA import alert listing or import refusal in SupplierRadar's records.

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gruvipa S.L.

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

2022

  1. Recall
    Recall (Class II), Cb1102006 bocata 120Finished product potentially adulterated with insect filth.
    Source
  2. Recall
    Recall (Class II), Cb1101001 barra xxlFinished product potentially adulterated with insect filth.
    Source
  3. Recall
    Recall (Class II), Cb1115007 silvestre cerealesFinished product potentially adulterated with insect filth.
    Source
  4. Recall
    Recall (Class II), Cb1102052 bocata especial casero'sFinished product potentially adulterated with insect filth.
    Source
  5. Recall
    Recall (Class II), CB1101004 BAGUETTE SUPER and CB1101005 BAGUETTE SUPER (34 u.)Finished product potentially adulterated with insect filth.
    Source
  6. Recall
    Recall (Class II), Cb1101006 barra larga con salvadoFinished product potentially adulterated with insect filth.
    Source

Questions about Gruvipa S.L.

Is Gruvipa S.L. on an FDA import alert?
No listing for Gruvipa S.L. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
Has FDA refused shipments from Gruvipa S.L.?
No FDA import refusals for Gruvipa S.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Gruvipa S.L.'s FEI number?
Gruvipa S.L.'s FDA Establishment Identifier (FEI) is 3014321363.

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Example subjectGruvipa S.L 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.