ImportRefusal LogoImportRefusal

BIOPURE EU LTD.

⚠️ Moderate Risk

FEI: 3012634653 • Guntramsdorf, Niederosterreich • AUSTRIA

FEI

FEI Number

3012634653

📍

Location

Guntramsdorf, Niederosterreich

🇦🇹

Country

AUSTRIA
🏢

Address

Rathaus Viertel 4, , Guntramsdorf, Niederosterreich, Austria

Moderate Risk

FDA Import Risk Assessment

30.9
LowModerateHighCritical

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

Statistics

4
Total Refusals
9
Unique Violations
12/2/2020
Latest Refusal
12/2/2020
Earliest Refusal

Score Breakdown

Violation Severity
47.8×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

164×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2184×

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.

23004×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

3204×

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.

3214×

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.

38634×

PLANT PART

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(C) of the FD&C Act in that the supplement contains an herb or other botanical described in section 201(ff)(1)(C), and the label or labeling of the supplement fails to identify any part of the plant from which the ingredient is derived.

38644×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

4824×

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.

754×

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).

Refusal History

DateProductViolationsDivision
12/2/2020
54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
321LACKS N/C
3863PLANT PART
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of West Coast Imports (DWCI)
12/2/2020
54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
321LACKS N/C
3863PLANT PART
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of West Coast Imports (DWCI)
12/2/2020
54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
321LACKS N/C
3863PLANT PART
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of West Coast Imports (DWCI)
12/2/2020
54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
16DIRECTIONS
218LIST INGRE
2300DIETARYLBL
320LACKS FIRM
321LACKS N/C
3863PLANT PART
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is BIOPURE EU LTD.'s FDA import refusal history?

BIOPURE EU LTD. (FEI: 3012634653) has 4 FDA import refusal record(s) in our database, spanning from 12/2/2020 to 12/2/2020.

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. BIOPURE EU LTD.'s FEI number is 3012634653.

What types of violations has BIOPURE EU LTD. received?

BIOPURE EU LTD. has been cited for 9 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 BIOPURE EU LTD. come from?

All FDA import refusal data for BIOPURE EU LTD. 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.