Hipp
⚠️ Moderate Risk
FEI: 3011900730 • Hurst Grove • UNITED KINGDOM
FEI Number
3011900730
Location
Hurst Grove
Country
UNITED KINGDOMAddress
The Stable Block, Standford Lane, Hurst Grove, , United Kingdom
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
FALSE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
NO ENGLISH
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
NUTR DEF
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the infant formula appears to adulterated in that it does not provide the nutrients required by 21 CFR 107.100
NUTR UNIT
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the infant formula appears to be misbranded within the meaning of Section 403 in that the labeling fails to use the proper units to declare the nutrients as specified in 21 CFR 107.10.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/19/2024 | 40NYT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED | 260FALSE | Division of Southeast Imports (DSEI) |
| 2/13/2024 | 40PGT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA | Division of Southeast Imports (DSEI) | |
| 12/27/2023 | 40PGT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA | 260FALSE | Division of Southeast Imports (DSEI) |
| 8/1/2023 | 40PFT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA | Division of Southeast Imports (DSEI) | |
| 10/20/2021 | 40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA | 260FALSE | Division of Southeast Imports (DSEI) |
| 12/18/2020 | 40BVT05RICE CEREAL (BABY) | 324NO ENGLISH | Division of West Coast Imports (DWCI) |
| 12/18/2020 | 40BVT05RICE CEREAL (BABY) | 324NO ENGLISH | Division of West Coast Imports (DWCI) |
| 6/5/2020 | 40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA | 260FALSE | Division of Southeast Imports (DSEI) |
| 4/29/2020 | 40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA | Division of Southeast Imports (DSEI) | |
| 4/24/2020 | 40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA | Division of Southeast Imports (DSEI) | |
| 11/22/2019 | 40NYY99OTHER FORMULA PRODUCTS, N.E.C., READY TO FEED | Division of Southeast Imports (DSEI) | |
| 7/13/2017 | 40NGT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), READY TO FEED | 473LABELING | Division of Northern Border Imports (DNBI) |
| 1/3/2017 | 03HMT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | 482NUTRIT LBL | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is Hipp's FDA import refusal history?
Hipp (FEI: 3011900730) has 13 FDA import refusal record(s) in our database, spanning from 1/3/2017 to 8/19/2024.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Hipp's FEI number is 3011900730.
What types of violations has Hipp received?
Hipp has been cited for 11 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Hipp come from?
All FDA import refusal data for Hipp is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.