ImportRefusal LogoImportRefusal

Bausch Health US., LLC.

⚠️ Moderate Risk

FEI: 3010446985 • Bridgewater, NJ • UNITED STATES

FEI

FEI Number

3010446985

📍

Location

Bridgewater, NJ

🇺🇸
🏢

Address

400 Somerset Corporate Blvd, , Bridgewater, NJ, United States

Moderate Risk

FDA Import Risk Assessment

49.1
LowModerateHighCritical

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

Statistics

6
Total Refusals
5
Unique Violations
4/8/2024
Latest Refusal
1/26/2016
Earliest Refusal

Score Breakdown

Violation Severity
72.2×40%
Refusal Volume
31.3×30%
Recency
50.4×20%
Frequency
7.3×10%
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

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).

1182×

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).

161×

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.

32801×

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.

5081×

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.

Refusal History

DateProductViolationsDivision
4/8/2024
61NCA05BUPROPION HCL (ANTI-DEPRESSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/26/2023
65RCY29TRETINOIN (REPLENISHER)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/9/2019
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
Division of Southeast Imports (DSEI)
4/12/2019
62VDY18ACYCLOVIR (ANTI-VIRAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/18/2018
86MUSFLUIDIC, PHACOEMULSIFICATION/PHACOFRAGMENTATION
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
1/26/2016
62ODY28ENALAPRIL MALEATE (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Bausch Health US., LLC.'s FDA import refusal history?

Bausch Health US., LLC. (FEI: 3010446985) has 6 FDA import refusal record(s) in our database, spanning from 1/26/2016 to 4/8/2024.

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. Bausch Health US., LLC.'s FEI number is 3010446985.

What types of violations has Bausch Health US., LLC. received?

Bausch Health US., 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 Bausch Health US., LLC. come from?

All FDA import refusal data for Bausch Health US., 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.