Teleflex Medical recalls

Teleflex Medical has 235 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 1 Jun 2022. 10 are still ongoing. The most frequent reason is sterility.

Total recalls235since 2012

Last 12 months0reported

Class I5021% of total

Ongoing10latest 1 Jun 2022

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 50 21%Class II 178 76%Class III 7 3%

Why teleflex medical is recalled

Product types

By year

202294%
202121%
20202310%
20193414%
201821%
2017209%
20162711%
20152812%
20148536%
201321%

Ongoing teleflex medical recalls

10 active

Reported	Class	Recall	Company	Reason	Where
1 Jun 2022Device	CLASS II	Teleflex Flex tube, Product #20011, sterile recalled by Teleflex Medical	Teleflex Medical	Sterility	Nationwide
1 Jun 2022Device	CLASS II	Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile recalled	Teleflex Medical	Sterility	Nationwide
3 Jun 2020Device	CLASS II	Sprotte Needle recalled by Teleflex Medical	Teleflex Medical	Sterility	Nationwide
3 Jun 2020Device	CLASS II	Sprotte Needle recalled by Teleflex Medical	Teleflex Medical	Sterility	Nationwide
25 Dec 2019Device	CLASS II	Arrow Ez-io Intraosseous Vascular Access System recalled	Teleflex Medical	Sterility	Nationwide
25 Dec 2019Device	CLASS II	Arrow Ez-io Intraosseous Vascular Access System recalled	Teleflex Medical	Sterility	Nationwide

All teleflex medical recalls, newest first

235 total

Reported	Class	Recall	Company	Reason	Where
1 Jun 2022Device	CLASS II	Teleflex Flex tube, Product #20011, sterile recalled by Teleflex Medical	Teleflex Medical	Sterility	Nationwide
1 Jun 2022Device	CLASS II	Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile recalled	Teleflex Medical	Sterility	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical	Teleflex Medical	Other	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical	Teleflex Medical	Other	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) recalled	Teleflex Medical	Other	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) recalled	Teleflex Medical	Other	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device recalled	Teleflex Medical	Other	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical	Teleflex Medical	Other	Nationwide
23 Feb 2022Device	CLASS I	Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical	Teleflex Medical	Other	Nationwide
31 Mar 2021Device	CLASS II	Pleur-evac Thoracic Catheters (Catheter, Irrigation) recalled	Teleflex Medical	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.