Unetixs Vascular recalls

Unetixs Vascular has 4 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 8 Mar 2023. 4 are still ongoing.

Total recalls4since 2023

Last 12 months0reported

Class I00% of total

Ongoing4latest 8 Mar 2023

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 4 100%Class III 0 0%

Why unetixs vascular is recalled

Other Reasons4100%

Product types

Heart & Vascular Devices4100%

By year

20234100%

Ongoing unetixs vascular recalls

4 active

Reported	Class	Recall	Company	Reason	Where
8 Mar 2023Device	CLASS II	MultiLab Series II LHS TI & ERGO non-invasive vascular recalled	Unetixs Vascular	Other	Nationwide
8 Mar 2023Device	CLASS II	MultiLab Series II REVO non-invasive vascular diagnostic device recalled	Unetixs Vascular	Other	Nationwide
8 Mar 2023Device	CLASS II	MultiLab Series II 2CP & 2CP Express non-invasive vascular recalled	Unetixs Vascular	Other	Nationwide
8 Mar 2023Device	CLASS II	MultiLab Series II Roodra non-invasive vascular diagnostic device recalled	Unetixs Vascular	Other	Nationwide

All unetixs vascular recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
8 Mar 2023Device	CLASS II	MultiLab Series II LHS TI & ERGO non-invasive vascular recalled	Unetixs Vascular	Other	Nationwide
8 Mar 2023Device	CLASS II	MultiLab Series II REVO non-invasive vascular diagnostic device recalled	Unetixs Vascular	Other	Nationwide
8 Mar 2023Device	CLASS II	MultiLab Series II 2CP & 2CP Express non-invasive vascular recalled	Unetixs Vascular	Other	Nationwide
8 Mar 2023Device	CLASS II	MultiLab Series II Roodra non-invasive vascular diagnostic device recalled	Unetixs Vascular	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.