Medtronic Vascular: 49 recalls on record

Recalls filed with 1 agency: FDA (49).

First recall on record: November 27, 2013. Most recent: October 9, 2019.

Risk classification: Class I: 47 · Class II: 1 · Class III: 1

Most recent recalls

DateAgencyProduct
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0, .070", REF SA6AL10. for cardiovascular useZ-2624-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F RBU4.5, .070", REF SA6RBU45. for cardiovascular u…Z-2667-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F, 3DRC 100CM .070", REF SA63DRC. for cardiovascula…Z-2564-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F LCB 90CM, .070", REF SA6LCBD. for cardiovascular…Z-2751-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP1.0 SH, .070", REF SA6CHAMP10SH. for cardiov…Z-2695-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F CHAMP3.5, .070", REF SA6CHAMP35. for cardiovascul…Z-2743-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F ERAD RIGHT SHORT TIP, .070", REF SA6ERADRST. for …Z-2730-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP2.0, 55CM.070", REF SA6CHAMP20K. for cardio…Z-2575-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F MAC5.0, .070", REF SA6MAC50. for cardiovascular u…Z-2733-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.5 SH, .070", REF SA6AL15SH. for cardiovascula…Z-2717-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F, IMA SH, 100CM, 070", REF SA6IMASH. for cardiovas…Z-2585-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. for cardiovascular useZ-2623-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F SCR3.5 SH, .070", REF SA6SCR35SH. for cardiovascu…Z-2738-2019
October 9, 2019FDASHERPA NX ACTIVE GUIDING CATHETER, 6F, RDND1 55CM .070", REF SA6RDND1K. for cardiovascu…Z-2563-2019
November 19, 2014FDAMedtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40KZ-0205-2015
March 5, 2014FDAMedtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The …Z-1121-2014
November 27, 2013FDAZINGER¿ Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZR…Z-0268-2014
November 27, 2013FDATHUNDER¿ Steerable Guidewire; Model: LVTNDR190S Medtronic guide wires are steerable g…Z-0267-2014
November 27, 2013FDATHUNDER¿ Extra Support Guidewire; Models: THNDR190J, THNDR190S, THNDR300J, THNDR300S …Z-0263-2014
November 27, 2013FDAProVia¿ CROSSING GUIDEWIRE; Models: 15PROV300HS, 3PROV180HS, 3PROV180SS, 3PROV300HS, 3PR…Z-0264-2014
November 27, 2013FDACOUGAR¿ Steerable Guidewire; Models: LVCLS190J, LVCLS190S, LVCXT190J, LVCXT190S Medtro…Z-0266-2014
November 27, 2013FDACougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300…Z-0261-2014
November 27, 2013FDAZinger¿ Stainless Steel Workhorse Guidewire; Models: ZNGRLS180HJ, ZNGRLS180HS, ZNGRMS180H…Z-0262-2014
November 27, 2013FDAATTAIN HYBRID¿ Guide Wire; Models: GWR419478, GWR419488, GWR419688 The Attain Hybrid g…Z-0265-2014

Questions about this company

How many recalls does Medtronic Vascular have?
Recalert has 49 U.S. recalls on record for Medtronic Vascular, published between November 27, 2013 and October 9, 2019.
Which agencies have handled Medtronic Vascular recalls?
Medtronic Vascular appears as the recalling firm in recalls from: FDA (49).

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