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Convatec Dominican Republic, Inc.

⚠️ Moderate Risk

FEI: 3003264198 • Haina San Cristobal • DOMINICAN REPUBLIC

FEI

FEI Number

3003264198

📍

Location

Haina San Cristobal

🇩🇴
🏢

Address

Carretera Sanchez, Km. 18.5, PARQUE INDUSTRIAL ITABO, S.A., Buildings 8A, 23, 29, 30, Haina San Cristobal, , Dominican Republic

Moderate Risk

FDA Import Risk Assessment

43.9
LowModerateHighCritical

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

Statistics

12
Total Refusals
5
Unique Violations
12/14/2023
Latest Refusal
10/28/2008
Earliest Refusal

Score Breakdown

Violation Severity
54.7×40%
Refusal Volume
41.3×30%
Recency
44.3×20%
Frequency
7.9×10%
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

1184×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32804×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3414×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5084×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

2373×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
12/14/2023
79NADDRESSING, WOUND, OCCLUSIVE
508NO 510(K)
Division of Southeast Imports (DSEI)
12/14/2023
79NADDRESSING, WOUND, OCCLUSIVE
508NO 510(K)
Division of Southeast Imports (DSEI)
11/25/2019
79NADDRESSING, WOUND, OCCLUSIVE
237NO PMA
Division of Southeast Imports (DSEI)
11/25/2019
78FONBAG, DRAINAGE, WITH ADHESIVE, OSTOMY
237NO PMA
Division of Southeast Imports (DSEI)
11/25/2019
79NADDRESSING, WOUND, OCCLUSIVE
237NO PMA
Division of Southeast Imports (DSEI)
5/15/2018
79FRODRESSING, WOUND, DRUG
508NO 510(K)
Division of Southeast Imports (DSEI)
5/15/2018
79FRODRESSING, WOUND, DRUG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/28/2018
79FRODRESSING, WOUND, DRUG
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
2/28/2018
79NADDRESSING, WOUND, OCCLUSIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
2/28/2018
79NADDRESSING, WOUND, OCCLUSIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
2/14/2018
79NADDRESSING, WOUND, OCCLUSIVE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/28/2008
78EZQPOUCH, COLOSTOMY
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Convatec Dominican Republic, Inc.'s FDA import refusal history?

Convatec Dominican Republic, Inc. (FEI: 3003264198) has 12 FDA import refusal record(s) in our database, spanning from 10/28/2008 to 12/14/2023.

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. Convatec Dominican Republic, Inc.'s FEI number is 3003264198.

What types of violations has Convatec Dominican Republic, Inc. received?

Convatec Dominican Republic, Inc. has been cited for 5 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 Convatec Dominican Republic, Inc. come from?

All FDA import refusal data for Convatec Dominican Republic, Inc. 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.