Medtronic Cardiovascular Surgery-the Heart Valve Division recalls

Medtronic Cardiovascular Surgery-the Heart Valve Division has 4 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 24 Aug 2016.

Total recalls4since 2014

Last 12 months0reported

Class I125% of total

Ongoing0latest 24 Aug 2016

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 1 25%Class II 3 75%Class III 0 0%

Why medtronic cardiovascular surgery-the heart valve division is recalled

Other Reasons375%
Particulate Matter125%

Product types

Heart & Vascular Devices375%
Other Medical Devices125%

By year

2016125%
2015125%
2014250%

All medtronic cardiovascular surgery-the heart valve division recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
24 Aug 2016Device	CLASS II	Medtronic EnVeo R Delivery Catheter System (DCS) recalled	Medtronic Cardiovascular Surgery-the Heart Valve Division	Other	PR
12 Aug 2015Device	CLASS I	EnVeo R Loading System recalled by Medtronic Cardiovascular	Medtronic Cardiovascular Surgery-the Heart Valve Division	Particulate Matter	Nationwide
17 Sep 2014Device	CLASS II	Hancock Apical Left Ventricle Connector recalled	Medtronic Cardiovascular Surgery-the Heart Valve Division	Other	MD, TX
12 Feb 2014Device	CLASS II	Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic recalled	Medtronic Cardiovascular Surgery-the Heart Valve Division	Other	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.