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SHS International, Ltd. dba Nutricia Liverpool

⚠️ Moderate Risk

FEI: 3002809433 • Liverpool, LIV • UNITED KINGDOM

FEI

FEI Number

3002809433

📍

Location

Liverpool, LIV

🇬🇧
🏢

Address

100 Wavertree Boulevard, Merseyside, Liverpool, LIV, United Kingdom

Moderate Risk

FDA Import Risk Assessment

34.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

12
Total Refusals
7
Unique Violations
10/4/2011
Latest Refusal
5/13/2003
Earliest Refusal

Score Breakdown

Violation Severity
52.7×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
14.3×10%
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

558×

OMITTED

The article is subject to refusal of admission pursuant Section 801(a)(3) of the FD&C Act in that it appears that a valuable constituent of the article has been in whole or in part omitted or abstracted from the article.

4822×

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.

3211×

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.

2181×

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.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

3201×

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.

Refusal History

DateProductViolationsDivision
10/4/2011
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)
6/20/2008
40CHT99FORMULA PRODUCTS (MILK AND MILK SUBSTITUTES) (BABY)
482NUTRIT LBL
New York District Office (NYK-DO)
6/20/2008
40CHT99FORMULA PRODUCTS (MILK AND MILK SUBSTITUTES) (BABY)
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
11/18/2004
41BYY99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
218LIST INGRE
320LACKS FIRM
321LACKS N/C
New Orleans District Office (NOL-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
54YGT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)
5/13/2003
41GEY99MEDICAL FOODS, N.E.C.
55OMITTED
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is SHS International, Ltd. dba Nutricia Liverpool's FDA import refusal history?

SHS International, Ltd. dba Nutricia Liverpool (FEI: 3002809433) has 12 FDA import refusal record(s) in our database, spanning from 5/13/2003 to 10/4/2011.

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. SHS International, Ltd. dba Nutricia Liverpool's FEI number is 3002809433.

What types of violations has SHS International, Ltd. dba Nutricia Liverpool received?

SHS International, Ltd. dba Nutricia Liverpool has been cited for 7 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 SHS International, Ltd. dba Nutricia Liverpool come from?

All FDA import refusal data for SHS International, Ltd. dba Nutricia Liverpool 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.