Hipp UK Limited Hurst Grove
FDA import alert and refusal historyReading, United KingdomFEI 3041692759
Recorded by FDA as HIPP UK LIMITED HURST GROVE
As of October 26, 2026, Hipp UK Limited Hurst Grove is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 15, 2026, 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 soups and soup mix (baby) · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hipp UK Limited Hurst Grove
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vegetable soups and soup mix (baby)NO PROCESSEntry SCS-8130531-7Source
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 Hipp UK Limited Hurst Grove
- Is Hipp UK Limited Hurst Grove on an FDA import alert?
- No listing for Hipp UK Limited Hurst Grove appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the United Kingdom page.
- Has FDA refused shipments from Hipp UK Limited Hurst Grove?
- Yes. FDA refused 1 shipment line from Hipp UK Limited Hurst Grove on September 15, 2026. The most recent, on September 15, 2026, was vegetable soups and soup mix (baby), charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Hipp UK Limited Hurst Grove's shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
- What is Hipp UK Limited Hurst Grove's FEI number?
- Hipp UK Limited Hurst Grove's FDA Establishment Identifier (FEI) is 3041692759.
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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.