Vitreq Bv recalls

Vitreq Bv has 16 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 5 Feb 2020. The most frequent reason is sterility.

Total recalls16since 2020

Last 12 months0reported

Class I00% of total

Ongoing0latest 5 Feb 2020

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 16 100%Class III 0 0%

Why vitreq bv is recalled

Sterility16100%

Product types

Syringes & Needles1063%
Heart & Vascular Devices638%

By year

202016100%

All vitreq bv recalls, newest first

16 total

Reported	Class	Recall	Company	Reason	Where
5 Feb 2020Device	CLASS II	Blunt Needles with luer-lock connector recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	VitreQ BF Blunt Needles recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	VFI Cannula recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	Blunt Needles with luer-lock connector recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	Silicone Tipped Cannula-CN23.D01 recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	Pick Needles recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	PFC Injection Needle recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	VitreQ BF Blunt Needles-.D51 GITN recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	Silicone Tipped Cannula recalled by Vitreq Bv	Vitreq Bv	Sterility	Nationwide
5 Feb 2020Device	CLASS II	PFC Injection Needle recalled by Vitreq Bv	Vitreq Bv	Sterility	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.