Covidien Medtronic recalls

Covidien Medtronic has 55 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 25 Jul 2018. 14 are still ongoing. The most frequent reason is packaging defects.

Total recalls55since 2017

Last 12 months0reported

Class I00% of total

Ongoing14latest 25 Jul 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 55 100%Class III 0 0%

Why covidien medtronic is recalled

Product types

By year

20185498%
201712%

Ongoing covidien medtronic recalls

14 active

Reported	Class	Recall	Company	Reason	Where
25 Jul 2018Device	CLASS II	Tri-Staple 0 Black Intelligent Reload for use recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Curved Tip Articulating Vascular/Medium Reload recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Tri-Staple 0 Intelligent Reload for use recalled by Covidien Medtronic	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Tri-Staple 0 Curved Tip Intelligent Reload for use recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Extra Thick Black Articulating Reload recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Extra Thick Black Articulating Reload recalled	Covidien Medtronic	Packaging Defects	Nationwide

All covidien medtronic recalls, newest first

55 total

Reported	Class	Recall	Company	Reason	Where
25 Jul 2018Device	CLASS II	Tri-Staple 0 Black Intelligent Reload for use recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Curved Tip Articulating Vascular/Medium Reload recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Tri-Staple 0 Intelligent Reload for use recalled by Covidien Medtronic	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Tri-Staple 0 Curved Tip Intelligent Reload for use recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Extra Thick Black Articulating Reload recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Extra Thick Black Articulating Reload recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Articulating Vascular/Medium Loading Unit recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Endo GIA Articulating Medium/Thick Reload with Tri-StapleTechnology recalled	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Tri-Staple 0 Intelligent Reload for use recalled by Covidien Medtronic	Covidien Medtronic	Packaging Defects	Nationwide
25 Jul 2018Device	CLASS II	Tri-Staple 0 Curved Tip Intelligent Reload for use recalled	Covidien Medtronic	Packaging Defects	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.