Covidien LP
⚠️ Moderate Risk
FEI: 1282497 • Mansfield, MA • UNITED STATES
FEI Number
1282497
Location
Mansfield, MA
Country
UNITED STATESAddress
15 Hampshire St, , Mansfield, MA, 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).
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.
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.
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.
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.
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.
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/14/2022 | 79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | Division of Southeast Imports (DSEI) | |
| 7/14/2022 | 79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | Division of Southeast Imports (DSEI) | |
| 1/27/2017 | 79GDWSTAPLE, IMPLANTABLE | New Orleans District Office (NOL-DO) | |
| 1/27/2017 | 79GEIDEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | New Orleans District Office (NOL-DO) | |
| 4/17/2014 | 73BZDVENTILATOR, NON-CONTINUOUS (RESPIRATOR) | 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 | 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 | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79LRPTRAY, SURGICAL | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79FRODRESSING, WOUND, DRUG | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79EFQSPONGE, GAUZE | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 80DWLSTOCKING, MEDICAL SUPPORT | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79KMFBANDAGE, LIQUID | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79MGPDRESSING, WOUND AND BURN, OCCLUSIVE | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 80DWLSTOCKING, MEDICAL SUPPORT | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 80DWLSTOCKING, MEDICAL SUPPORT | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79KMFBANDAGE, LIQUID | Chicago District Office (CHI-DO) | |
| 8/13/2002 | 79LRPTRAY, SURGICAL | Chicago District Office (CHI-DO) | |
| 5/11/2002 | 78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER | 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.