Angiodynamics Inc. (Navilyst Medical Inc.) recalls

Angiodynamics Inc. (Navilyst Medical Inc.) has 78 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 6 Oct 2021.

Total recalls78since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 6 Oct 2021

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 78 100%Class III 0 0%

Why angiodynamics inc. (navilyst medical inc.) is recalled

Product types

By year

202134%
20191114%
20184254%
20171519%
201679%

All angiodynamics inc. (navilyst medical inc.) recalls, newest first

78 total

Reported	Class	Recall	Company	Reason	Where
6 Oct 2021Device	CLASS II	Xcela PICC with Pasv Valve Technology/Kit 5 F recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Labeling Errors	NY
28 Apr 2021Device	CLASS II	Smart Port CT-Implantable Port recalled by Angiodynamics Inc. (Navilyst	Angiodynamics Inc. (Navilyst Medical Inc.)	Sterility	Nationwide
28 Apr 2021Device	CLASS II	AngioDynamics Safe Sheath Ultralite recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Sterility	Nationwide
27 Nov 2019Device	CLASS II	Starburst Talon Semi-Flex Electrosurgical Device recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Labeling Errors	5 states
27 Nov 2019Device	CLASS II	Bioflo 8f Single Plastic Non-filled recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Foreign Material	Nationwide
27 Nov 2019Device	CLASS II	Xcela, 8f Single Plastic Port Filled, Valved, Upn H965440400 recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Foreign Material	Nationwide
27 Nov 2019Device	CLASS II	Bioflo 8f Single Plastic Filled recalled by Angiodynamics Inc. (Navilyst	Angiodynamics Inc. (Navilyst Medical Inc.)	Foreign Material	Nationwide
27 Nov 2019Device	CLASS II	Bioflo 8f Single Plastic Filled recalled by Angiodynamics Inc. (Navilyst	Angiodynamics Inc. (Navilyst Medical Inc.)	Foreign Material	Nationwide
27 Nov 2019Device	CLASS II	Bioflo 8f Single Titanium Non- Filled recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Device Malfunction	Nationwide
12 Jun 2019Device	CLASS II	AngioDynamics Solero Microwave Tissue Ablation (MTA) System recalled	Angiodynamics Inc. (Navilyst Medical Inc.)	Device Malfunction	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.