Terumo Medical Corporation
⚠️ Moderate Risk
FEI: 1118880 • Elkton, MD • UNITED STATES
FEI Number
1118880
Location
Elkton, MD
Country
UNITED STATESAddress
950 Elkton Blvd, , Elkton, MD, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/24/2005 | 80FMFSYRINGE, PISTON | 341REGISTERED | Cincinnati District Office (CIN-DO) |
| 5/1/2003 | 80FMINEEDLE, HYPODERMIC, SINGLE LUMEN | Chicago District Office (CHI-DO) | |
| 5/1/2003 | 80FMFSYRINGE, PISTON | Chicago District Office (CHI-DO) | |
| 3/31/2003 | 80FMINEEDLE, HYPODERMIC, SINGLE LUMEN | Chicago District Office (CHI-DO) | |
| 3/31/2003 | 80FMFSYRINGE, PISTON | Chicago District Office (CHI-DO) | |
| 3/31/2003 | 80FMINEEDLE, HYPODERMIC, SINGLE LUMEN | Chicago District Office (CHI-DO) | |
| 3/31/2003 | 80FMFSYRINGE, PISTON | Chicago District Office (CHI-DO) | |
| 3/19/2003 | 80FMINEEDLE, HYPODERMIC, SINGLE LUMEN | Chicago District Office (CHI-DO) | |
| 12/3/2002 | 80FMFSYRINGE, PISTON | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Terumo Medical Corporation's FDA import refusal history?
Terumo Medical Corporation (FEI: 1118880) has 9 FDA import refusal record(s) in our database, spanning from 12/3/2002 to 10/24/2005.
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. Terumo Medical Corporation's FEI number is 1118880.
What types of violations has Terumo Medical Corporation received?
Terumo Medical Corporation 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 Terumo Medical Corporation come from?
All FDA import refusal data for Terumo Medical Corporation 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.