Terumo Cardiovascular Systems Corporation: 161 recalls on record

Recalls filed with 1 agency: FDA (161).

First recall on record: June 27, 2012. Most recent: July 2, 2025.

Risk classification: Class II: 160 · Class III: 1

Most recent recalls

DateAgencyProduct
July 24, 2013FDACDI Blood Parameter Monitoring System 500 with Venous blood parameter module. Intended…Z-1734-2013
July 24, 2013FDACDI Blood Parameter Monitoring System 500 with Arterial blood parameter modules and Hemat…Z-1731-2013
July 24, 2013FDACDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter module…Z-1732-2013
July 24, 2013FDACDI Blood Parameter Monitoring System 500 with Arterial blood parameter module. Intend…Z-1733-2013
July 24, 2013FDACDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter module…Z-1730-2013
July 3, 2013FDASarns " TCM II Temperature Control Module The Sarns" TCM II Temperature Control Module…Z-1569-2013
February 20, 2013FDATerumo CDI 101 Hematocrit/Oxygen Saturation Monitoring System. Monitors blood/oxygen satu…Z-0802-2013
January 23, 2013FDASarns flexible arterial cannula, 8.0 mm (24 Fr) with 3/8in connector, suture ring, 9.5in …Z-0668-2013
January 23, 2013FDASarns high-flow aortic arch cannula, 5.2 mm (16 Fr) OD with 3/8in connector, 7.5in (19 cm…Z-0669-2013
January 23, 2013FDASarns high-flow aortic arch cannula, 6.5 mm (20 Fr) OD with 3/8in connector, 11in (28 cm)…Z-0671-2013
January 23, 2013FDASarns flexible arterial cannula, 7.3 mm (22 Fr) OD with 3/8in connector, suture ring, 9.5…Z-0667-2013
January 23, 2013FDASarns high-flow aortic arch cannula, 6.5 mm (20 Fr) OD with 3/8in connector, 11in (28 cm)…Z-0670-2013
January 23, 2013FDASarns flexible arterial cannula, 6.7 mm (20Fr) OD with 3/8 in. connector, suture ring, 9.…Z-0666-2013
December 12, 2012FDA24 Fr 8mm Soft Flow Ang Wire W/L The Sarns Aortic Cannula is indicated for use in perf…Z-0461-2013
December 12, 2012FDA24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Cannula is indicated for use in perfusion…Z-0462-2013
December 12, 2012FDA24 Fr 8mm Sft Flow Straight The Sarns Aortic Cannula is indicated for use in perfusion…Z-0458-2013
December 12, 2012FDA24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Cannula is indicated for use in perfu…Z-0457-2013
December 12, 2012FDA18 Fr 6mm Sft Flow Ang Wire W/L The Sarns Aortic Cannula is indicated for use in perfu…Z-0460-2013
December 12, 2012FDA24 Fr 8mm Sft Flow Str Wire W/L The Sarns Aortic Cannula is indicated for use in perfu…Z-0456-2013
December 12, 2012FDA18 Fr 6mm Sft Flow Angled Wire The Sarns Aortic Cannula is indicated for use in perfus…Z-0459-2013
December 5, 2012FDA100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion S…Z-0435-2013
December 5, 2012FDA220/240V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion S…Z-0436-2013
November 21, 2012FDAHX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management System is a selfcontain…Z-0278-2013
November 21, 2012FDAPerfusion System 8000, base 5 pump, 100V safety monitor included The Sarns" Modular Pe…Z-0285-2013
November 21, 2012FDAPerfusion System 8000, base 4 pump, 100V safety monitor included The Sarns" Modular Pe…Z-0284-2013

Questions about this company

How many recalls does Terumo Cardiovascular Systems Corporation have?
Recalert has 161 U.S. recalls on record for Terumo Cardiovascular Systems Corporation, published between June 27, 2012 and July 2, 2025.
Which agencies have handled Terumo Cardiovascular Systems Corporation recalls?
Terumo Cardiovascular Systems Corporation appears as the recalling firm in recalls from: FDA (161).

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