BEUDAMED
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    Cordis CROSSOVER. Cordis CROSSOVER Sheath Introducer. Thomas Medical Products, Inc. 65 Great Valley Parkway, Malvern, PA 19355 USA. Distributed by Cordis Corporation, 14201 North West 60th Avenue, Miami Lakes, Florida 33014 USA Vital Signs, Ltd. 13-14 Eldon Way Lineside Industrial Estate, Littlehampton, West Sussex, UK. The Cordis CROSSOVER Sheath Introducer is intended for use in arterial and venous procedures requiring percutaneous introduction of therapeutic or diagnostic intravascular devices or fluids.

    FDA Recall
    Terminated ·Cordis Corporation·Product code DYB·October 15, 2009

    SUPER TORQUE MB Angiographic Catheter product is labeled in part: "***5F (1.65 mm)***110 cm .038" (0.97 mm)***MULTIPURPOSE A SUPER TORQUE MB***Max. 1200 psi (8274 kPa)***Markers***OPEN end***Sideholes***SPECIAL***Angiographic Catheter*** REF Cat No.***Lot***Use By***Sterile EO***Assembled in Mexico Cordis Corporation, 14201 NW 60th Ave. Miami Lakes, Florida 33014, USA***EC***REP*** Cordis Cashel, Cahir Road Cashel, Co Tipperary, Ireland***Cordis***a Johnson&Johnson company***" UPN SRD5724MB, No MB 2, Length, cm 100, Sideholes 2. UPN SRD5727MB, No MB 4, Length, cm 80, Sideholes 4. Cordis SUPER TORQUE MB angiographic catheters with Market Bands are designed to provide angiographic visualization and linear measurement of the vasculature when combined with the delivery of radiopaque contrast media to selected sites in the vascular system.

    FDA Recall
    Terminated ·Cordis Corporation·Product code DQO·November 21, 2011

    SUPER TORQUE MB Angiographic Catheter product is labeled in part: "***5F (1.65 mm)***110 cm .038" (0.97 mm)***PIG***Max. 1200 psi (8274 kPa)***Markers***Open End 6 Sideholes***Angiographic Catheter*** REF Cat No.***Lot***Use By***Assembled in Mexico Cordis Corporation, 14201 NW 60th Ave. Miami Lakes, Florida 33014, USA***EC***REP*** Cordis Cashel, Cahir Road Cashel, Co Tipperary, Ireland***Cordis***a Johnson&Johnson company***" UPN H739532598A3, Cat No 532-598A, No. MB 10, French Size 5, Shape (PIG), Length cm 110, Flow Rate, ml/sec, 18, Sideholes 6. UPN H739532598B3, Cat No 532-598B, No. MB 20, French Size 5, Shape (PIG), Length cm 110, Flow Rate, ml/sec, 18, Sideholes 6. UPN H73953298C3, Cat No 532-598C, No MB 20 French Size 5, Shape (PIG), Length, cm 65, Flow Rate, ml/sec, 30, Side Holes 6. UPN H73953298D3, Cat No 532-598D, No MB 2 French Size 5, Shape (PIG), Length , cm 70, Flow Rate, ml/sec, 30, Side Holes 10. Cordis SUPER TORQUE MB angiographic catheters with Market Bands are designed to provide angiographic visualization and linear measurement of the vasculature when combined with the delivery of radiopaque contrast media to selected sites in the vascular system.

    FDA Recall
    Terminated ·Cordis Corporation·Product code DQO·November 21, 2011

    CORDIS-SV-5 Steerable Guidewire, 300 cm.,5 Steerable Guidewires,Cordis a Johnson Johnson Company ,ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA., Catalog # 503558X

    FDA Recall
    Terminated ·Cordis Corporation·Product code DXQ·July 21, 2006

    CORDIS SV-8 Steerable Guidewire, 180 cm. , 5 Steerable Guidewires, Cordis a Johnson Johnson Company, ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA., Catalog # 503658

    FDA Recall
    Terminated ·Cordis Corporation·Product code DXQ·July 21, 2006

    CORDIS SV-8 Steerable Guidewire, 300 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson Company ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA, Catalog # 503658X

    FDA Recall
    Terminated ·Cordis Corporation·Product code DXQ·July 21, 2006

    CORDIS SV-5 Steerable Guidewire, 180 cm., 5 Steerable Guidewires, Cordis a Johnson Johnson Company, ENDOVASCULAR, Manufactured for: Cordis Corporation, Miami, FL 33102-5700. USA, Catalog # 503558.

    FDA Recall
    Terminated ·Cordis Corporation·Product code DXQ·July 21, 2006

    CORDIS "Dura Star" 2.25 x 25 Dilatation Catheter, Catalog # 70125225, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Fire Star" 3.50 x 10 Dilatation Catheter, Catalog # 80110350, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 3.50 x 15 Dilatation Catheter, Catalog # 70115350, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Fire Star" 2.25 x 10 Dilatation Catheter, Catalog # 80110225, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 4.00 x 15 Dilatation Catheter, Catalog # 70115400, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 3.25 x 15 Dilatation Catheter, Catalog # 70115325, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 3.75 x 25 Dilatation Catheter, Catalog # 70125375, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 2.75 x 25 Dilatation Catheter, Catalog # 70125275, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 2.75 x 15 Dilatation Catheter, Catalog # 70115275, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 2.50 x 10 Dilatation Catheter, Catalog # 70110250, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 3.25 x 25 Dilatation Catheter, Catalog # 70125325, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Dura Star" 3.00 x 10 Dilatation Catheter, Catalog # 70110300, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008

    CORDIS "Fire Star" 2.50 x 20 Dilatation Catheter, Catalog # 80120250, Distributed by Cordis Corporation, Miami Lakes, FL 33014

    FDA Recall
    Terminated ·Cordis Corporation·Product code LOX·January 14, 2008