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ETHICON, LLC

⚠️ Moderate Risk

FEI: 3007791599 • Guaynabo, PR • UNITED STATES

FEI

FEI Number

3007791599

📍

Location

Guaynabo, PR

🇺🇸
🏢

Address

475 Calle C Ste 401, , Guaynabo, PR, United States

Moderate Risk

FDA Import Risk Assessment

44.6
LowModerateHighCritical

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

Statistics

9
Total Refusals
5
Unique Violations
7/19/2024
Latest Refusal
2/28/2020
Earliest Refusal

Score Breakdown

Violation Severity
50.6×40%
Refusal Volume
37.0×30%
Recency
56.2×20%
Frequency
20.5×10%
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

32807×

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.

1186×

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).

3412×

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).

5082×

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.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

Refusal History

DateProductViolationsDivision
7/19/2024
79GAKSUTURE, ABSORBABLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Northeast Imports (DNEI)
1/5/2024
79GAMSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
9/29/2023
79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
3280FRNMFGREG
Division of Southeast Imports (DSEI)
3/27/2023
79GDWSTAPLE, IMPLANTABLE
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
3/1/2021
79GDWSTAPLE, IMPLANTABLE
118NOT LISTED
Division of Southeast Imports (DSEI)
3/1/2021
79GDWSTAPLE, IMPLANTABLE
118NOT LISTED
Division of Southeast Imports (DSEI)
2/19/2021
79GAMSUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
118NOT LISTED
223FALSE
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
2/28/2020
79GAWSUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
2/28/2020
79GAWSUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ETHICON, LLC's FDA import refusal history?

ETHICON, LLC (FEI: 3007791599) has 9 FDA import refusal record(s) in our database, spanning from 2/28/2020 to 7/19/2024.

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. ETHICON, LLC's FEI number is 3007791599.

What types of violations has ETHICON, LLC received?

ETHICON, LLC 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 ETHICON, LLC come from?

All FDA import refusal data for ETHICON, LLC 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.