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Henry Schein Inc.

⚠️ Moderate Risk

FEI: 1000522050 • Melville, NY • UNITED STATES

FEI

FEI Number

1000522050

📍

Location

Melville, NY

🇺🇸
🏢

Address

135 Duryea Rd, , Melville, NY, United States

Moderate Risk

FDA Import Risk Assessment

30.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
7/28/2020
Latest Refusal
11/18/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
1.7×10%
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

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).

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.

751×

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).

Refusal History

DateProductViolationsDivision
7/28/2020
80FXXMASK, SURGICAL
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/24/2011
80KGXTAPE AND BANDAGE, ADHESIVE
118NOT LISTED
New Orleans District Office (NOL-DO)
11/18/2002
60QDY40LIDOCAINE HCL (ANESTHETIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Henry Schein Inc.'s FDA import refusal history?

Henry Schein Inc. (FEI: 1000522050) has 3 FDA import refusal record(s) in our database, spanning from 11/18/2002 to 7/28/2020.

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. Henry Schein Inc.'s FEI number is 1000522050.

What types of violations has Henry Schein Inc. received?

Henry Schein Inc. has been cited for 3 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 Henry Schein Inc. come from?

All FDA import refusal data for Henry Schein 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.