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PURDUE PHARMA

⚠️ High Risk

FEI: 3021520194 • North York, Ontario • CANADA

FEI

FEI Number

3021520194

📍

Location

North York, Ontario

🇨🇦

Country

CANADA
🏢

Address

3381 Steeles Ave E, , North York, Ontario, Canada

High Risk

FDA Import Risk Assessment

56.6
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

2
Total Refusals
2
Unique Violations
12/21/2025
Latest Refusal
10/3/2023
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
17.7×30%
Recency
98.8×20%
Frequency
9.0×10%
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

752×

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).

1181×

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).

Refusal History

DateProductViolationsDivision
12/21/2025
65DCE99OXYTOCIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/3/2023
62FCK34POVIDONE IODINE (ANTI-INFECTIVE, TOPICAL)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PURDUE PHARMA's FDA import refusal history?

PURDUE PHARMA (FEI: 3021520194) has 2 FDA import refusal record(s) in our database, spanning from 10/3/2023 to 12/21/2025.

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. PURDUE PHARMA's FEI number is 3021520194.

What types of violations has PURDUE PHARMA received?

PURDUE PHARMA has been cited for 2 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 PURDUE PHARMA come from?

All FDA import refusal data for PURDUE PHARMA 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.