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Covidien LP

⚠️ Moderate Risk

FEI: 1282497 • Mansfield, MA • UNITED STATES

FEI

FEI Number

1282497

📍

Location

Mansfield, MA

🇺🇸
🏢

Address

15 Hampshire St, , Mansfield, MA, United States

Moderate Risk

FDA Import Risk Assessment

44.0
LowModerateHighCritical

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

Statistics

36
Total Refusals
9
Unique Violations
7/14/2022
Latest Refusal
5/11/2002
Earliest Refusal

Score Breakdown

Violation Severity
47.0×40%
Refusal Volume
58.1×30%
Recency
30.0×20%
Frequency
17.8×10%
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

11827×

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).

34117×

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).

1796×

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.

32804×

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.

5082×

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.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

33401×

DE/RX KIT

The article appears to be a combination medical device/prescription drug kit for which the prescription drug component was manufactured in the U.S., is 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.

20601×

AGRINSULIN

The article appears to be composed wholly or partly of insulin manufactured in the US and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for a medical emergency

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

Refusal History

DateProductViolationsDivision
7/14/2022
79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/14/2022
79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
1/27/2017
79GDWSTAPLE, IMPLANTABLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
New Orleans District Office (NOL-DO)
1/27/2017
79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
118NOT LISTED
3280FRNMFGREG
341REGISTERED
New Orleans District Office (NOL-DO)
4/17/2014
73BZDVENTILATOR, NON-CONTINUOUS (RESPIRATOR)
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)
11/20/2012
66VAA99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
Florida District Office (FLA-DO)
9/7/2011
80LDQDEVICE, GENERAL MEDICAL
118NOT LISTED
New Orleans District Office (NOL-DO)
8/4/2008
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
118NOT LISTED
Chicago District Office (CHI-DO)
5/23/2008
80FMINEEDLE, HYPODERMIC, SINGLE LUMEN
118NOT LISTED
3340DE/RX KIT
508NO 510(K)
Chicago District Office (CHI-DO)
3/12/2004
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
2060AGRINSULIN
Chicago District Office (CHI-DO)
3/12/2004
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
179AGR RX
Chicago District Office (CHI-DO)
8/27/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
179AGR RX
Chicago District Office (CHI-DO)
8/27/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
179AGR RX
Chicago District Office (CHI-DO)
6/26/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
179AGR RX
Chicago District Office (CHI-DO)
5/1/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
179AGR RX
Chicago District Office (CHI-DO)
5/1/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
118NOT LISTED
Chicago District Office (CHI-DO)
3/31/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
118NOT LISTED
Chicago District Office (CHI-DO)
3/31/2003
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
118NOT LISTED
Chicago District Office (CHI-DO)
12/3/2002
62FAK23ISOPROPYL ALCOHOL (ANTI-INFECTIVE, TOPICAL)
179AGR RX
Chicago District Office (CHI-DO)
10/21/2002
78EZLCATHETER, RETENTION TYPE, BALLOON
126FAILS STD
Chicago District Office (CHI-DO)
9/11/2002
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
223FALSE
Los Angeles District Office (LOS-DO)
8/13/2002
79MGPDRESSING, WOUND AND BURN, OCCLUSIVE
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79LRPTRAY, SURGICAL
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79FRODRESSING, WOUND, DRUG
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79EFQSPONGE, GAUZE
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
80DWLSTOCKING, MEDICAL SUPPORT
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79KMFBANDAGE, LIQUID
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79MGPDRESSING, WOUND AND BURN, OCCLUSIVE
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
80DWLSTOCKING, MEDICAL SUPPORT
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
80DWLSTOCKING, MEDICAL SUPPORT
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79KMFBANDAGE, LIQUID
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
8/13/2002
79LRPTRAY, SURGICAL
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)
5/11/2002
78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
118NOT LISTED
341REGISTERED
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Covidien LP's FDA import refusal history?

Covidien LP (FEI: 1282497) has 36 FDA import refusal record(s) in our database, spanning from 5/11/2002 to 7/14/2022.

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. Covidien LP's FEI number is 1282497.

What types of violations has Covidien LP received?

Covidien LP has been cited for 9 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 Covidien LP come from?

All FDA import refusal data for Covidien LP 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.