Medical DeviceAug 19, 2026
Terumo Medical GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box recall — FDA Z-2930-2026
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Class IIFDA: OngoingTerumo Medical Corporation
Recall history in this database
Classification mix: Class II: 10, Class I: 3.
Medical DeviceJul 31, 2019
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280 recall — FDA Z-2003-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Needle, 23G x 1", Product Code NN2325R recall — FDA Z-2005-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Sur-vet Needle, 20G x 1", Product Code 100204 recall — FDA Z-1998-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Sur-vet Needle, 22G x 1", Product Code 100211 recall — FDA Z-1999-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215 recall — FDA Z-2000-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Needle, 18G x 1", Product Code NN1825R recall — FDA Z-2004-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Needle, 30G x 1/2", Product Code NN3013R recall — FDA Z-2006-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279 recall — FDA Z-2002-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJul 31, 2019
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220 recall — FDA Z-2001-2019
There is a potential for a loss of package integrity that may compromise the sterility of the product.
Class IIFDA: TerminatedTerumo Medical Corporation
Medical DeviceJun 5, 2019
Terumo Medical SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425 recall — FDA Z-1374-2019
There is a potential for dislodgement of the tip from the outer diameter of the sheath resulting in a loss of the smooth transition from the surface of the tip to the outer surface of the…
Class IFDA: TerminatedTerumo Medical Corporation
Medical DeviceJun 5, 2019
Terumo Medical Portico Solo Re-Collapsible Access System , Model Numbers PRTSOLO-19 recall — FDA Z-1376-2019
There is a potential for dislodgement of the tip from the outer diameter of the sheath resulting in a loss of the smooth transition from the surface of the tip to the outer surface of the…
Class IFDA: TerminatedTerumo Medical Corporation
Medical DeviceJun 5, 2019
Terumo Medical SOLOPATH Re-Collapsible Access System, Model Numbers SR-1925, SR-1935 recall — FDA Z-1375-2019
There is a potential for dislodgement of the tip from the outer diameter of the sheath resulting in a loss of the smooth transition from the surface of the tip to the outer surface of the…
Class IFDA: TerminatedTerumo Medical Corporation
Understanding this recall history
This page summarizes recall records in which the official source identifies Terumo Medical Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.