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Morton Grove Pharmaceuticals, Inc.

⚠️ Moderate Risk

FEI: 1420913 • Morton Grove, IL • UNITED STATES

FEI

FEI Number

1420913

📍

Location

Morton Grove, IL

🇺🇸
🏢

Address

6451 Main St, , Morton Grove, IL, United States

Moderate Risk

FDA Import Risk Assessment

29.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
8/21/2009
Latest Refusal
4/14/2003
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
3.1×10%
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

1792×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

Refusal History

DateProductViolationsDivision
8/21/2009
60QDL07LIDOCAINE
179AGR RX
Southwest Import District Office (SWI-DO)
4/14/2003
61MDK30VALPROATE SODIUM (ANTI-CONVULSANT)
179AGR RX
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Morton Grove Pharmaceuticals, Inc.'s FDA import refusal history?

Morton Grove Pharmaceuticals, Inc. (FEI: 1420913) has 2 FDA import refusal record(s) in our database, spanning from 4/14/2003 to 8/21/2009.

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. Morton Grove Pharmaceuticals, Inc.'s FEI number is 1420913.

What types of violations has Morton Grove Pharmaceuticals, Inc. received?

Morton Grove Pharmaceuticals, Inc. has been cited for 1 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 Morton Grove Pharmaceuticals, Inc. come from?

All FDA import refusal data for Morton Grove Pharmaceuticals, 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.