Terumo Medical recalls

Terumo Medical has 39 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 19 Aug 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is sterility.

Total recalls39since 2013

Last 12 months1reported

Class I38% of total

Ongoing1latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 1Aug 0 0

Severity split

Class I 3 8%Class II 36 92%Class III 0 0%

Why terumo medical is recalled

Product types

By year

202613%
20191231%
201825%
20171949%
201625%
201513%
201325%

Ongoing terumo medical recalls

1 active

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Device	CLASS II	Glidesheath Slender A-kit 6f .021gw recalled by Terumo Medical	Terumo Medical	Packaging Defects	Nationwide

All terumo medical recalls, newest first

39 total

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Device	CLASS II	Glidesheath Slender A-kit 6f .021gw recalled by Terumo Medical	Terumo Medical	Packaging Defects	Nationwide
31 Jul 2019Device	CLASS II	Terumo Sur-vet Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Sur-vet Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Sur-vet Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Sur-vet Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Sur-vet Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
31 Jul 2019Device	CLASS II	Terumo Sur-vet Needle, Product recalled by Terumo Medical	Terumo Medical	Sterility	12 states
5 Jun 2019Device	CLASS I	Solopath Re-Collapsible Access System recalled by Terumo Medical	Terumo Medical	Other	Nationwide
5 Jun 2019Device	CLASS I	Portico Solo Re-Collapsible Access System recalled by Terumo Medical	Terumo Medical	Other	Nationwide
5 Jun 2019Device	CLASS I	Solopath Balloon Expandable TransFemoral System recalled	Terumo Medical	Other	Nationwide
11 Jul 2018Device	CLASS II	Angio-Seal Evolution Vascular Closure Device recalled by Terumo Medical	Terumo Medical	Sterility	12 states
7 Mar 2018Device	CLASS II	Destination Guiding Sheath catheter introducer recalled	Terumo Medical	Other	MD
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.025) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.021) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath - (0.025) recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath recalled	Terumo Medical	Sterility	Nationwide
20 Dec 2017Device	CLASS II	Glidesheath Slender Hydrophilic Coated Introducer Sheath recalled	Terumo 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.