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Purdue Pharma

⚠️ High Risk

FEI: 3003287869 • Pickering, Ontario • CANADA

FEI

FEI Number

3003287869

📍

Location

Pickering, Ontario

🇨🇦

Country

CANADA
🏢

Address

575 Granite Crt, , Pickering, Ontario, Canada

High Risk

FDA Import Risk Assessment

64.3
LowModerateHighCritical

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

Statistics

16
Total Refusals
4
Unique Violations
10/29/2025
Latest Refusal
6/22/2004
Earliest Refusal

Score Breakdown

Violation Severity
77.0×40%
Refusal Volume
45.6×30%
Recency
95.5×20%
Frequency
7.5×10%
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

7515×

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).

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).

32803×

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.

3421×

PERSONALRX

The article appears to be a drug which requires a prescription from your doctor.

Refusal History

DateProductViolationsDivision
10/29/2025
60CAQ48OXYMETAZOLINE HCL (ADRENERGIC)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Northern Border Imports (DNBI)
10/29/2025
64DAK01CARBOXYMETHYLCELLULOSE SODIUM, EMOLLIENT,LUBRICANT
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Northern Border Imports (DNBI)
9/10/2020
61TDI36PALONOSETRON HYDROCHLORIDE
118NOT LISTED
Division of Southeast Imports (DSEI)
3/18/2019
60MDA16OXYCODONE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/25/2016
60MCF08HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Seattle District Office (SEA-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
7/30/2013
60MCH25HYDROMORPHONE HYDROCHLORIDE (ANALGESIC, NARCOTIC)
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/23/2011
63HCA22SENNA (CATHARTIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
6/22/2004
60LAY99ANALGESIC, N.E.C.
342PERSONALRX
75UNAPPROVED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Purdue Pharma's FDA import refusal history?

Purdue Pharma (FEI: 3003287869) has 16 FDA import refusal record(s) in our database, spanning from 6/22/2004 to 10/29/2025.

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 3003287869.

What types of violations has Purdue Pharma received?

Purdue Pharma has been cited for 4 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.