SupplierRadar

Prihane pickles

FDA import alert and refusal historyKafr Qari'A, IsraelFEI 3013705238

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Example subjectPrihane pickle added to Import Alert 16-129 (red list)

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As of October 26, 2026, Prihane pickles is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 16, 2019, 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
Cucumbers (fruit used as vegetable) · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Prihane pickles

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

2019

  1. Import refusal
    Refused, Cucumbers (fruit used as vegetable)NO PROCESSEntry DP4-8257546-2
    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 Prihane pickles

Is Prihane pickles on an FDA import alert?
No listing for Prihane pickles appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Israel page.
Has FDA refused shipments from Prihane pickles?
Yes. FDA refused 1 shipment line from Prihane pickles on April 16, 2019. The most recent, on April 16, 2019, was cucumbers (fruit used as vegetable), charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Prihane pickles's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
What is Prihane pickles's FEI number?
Prihane pickles's FDA Establishment Identifier (FEI) is 3013705238.

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Example subjectPrihane pickle 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.