Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): 25 recalls on record

Recalls filed with 1 agency: FDA (25).

First recall on record: July 18, 2018. Most recent: June 28, 2023.

Risk classification: Class I: 13 · Class II: 11 · Class III: 1

Most recent recalls

DateAgencyProduct
June 28, 2023FDACRT-D DTBB1QQ VIVA QUAD S IS4/DF4 US, Model Number DTBB1QQ; Implantable Cardioverter Def…Z-1744-2023
June 28, 2023FDAICD-VR VISIA MRI AF S US/OUS DF4, Model Number DVFC3D4; Implantable Cardioverter Defibri…Z-1808-2023
June 28, 2023FDAICD-VR DVBC3D4 EVERA S DF4 GLOB, Model Number DVBC3D4; Implantable Cardioverter Defibril…Z-1800-2023
June 28, 2023FDAICD-DR DDMD3D4 PRIMO MRI, Model Number DDMD3D4; Implantable Cardioverter DefibrillatorsZ-1718-2023
June 28, 2023FDACRTD DTMC2QQ COMPIA MRI QUAD OUS DF4, Model Number DTMC2QQ; Implantable Cardioverter Def…Z-1773-2023
June 28, 2023FDAICD CROME VR MRI IS1 DF1, Model Number DVPC3D1; Implantable Cardioverter DefibrillatorsZ-1822-2023
June 28, 2023FDACRT-D DTBA1D1 VIVA XT IS1/DF1 US, Model Number DTBA1D1; Implantable Cardioverter Defibri…Z-1729-2023
June 28, 2023FDAICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter DefibrillatorsZ-1817-2023
June 28, 2023FDAICD-VR DVFB2D1 VISIA AF MRI XT OUS DF1, Model Number DVFB2D1; Implantable Cardioverter D…Z-1805-2023
August 17, 2022FDACrome Implantable Cardioverter Defibrillators: a. Crome VR ICD, Model Numbers: DVPC3D1, D…Z-1489-2022
August 17, 2022FDACobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CR…Z-1486-2022
August 17, 2022FDACobalt Implantable Cardioverter Defibrillators: a. Cobalt XT VR ICD, Model Numbers: DVPA2…Z-1485-2022
August 3, 2022FDACobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CR…Z-1480-2022
May 12, 2021FDACareLink SmartSync Device Manager (24970A). used to interrogate cardiac implantable elec…Z-1522-2021
July 15, 2020FDAAzure S DR MRI, Model Number W3DR01Z-2508-2020
July 15, 2020FDACareLink SmartSync Device Manager, Model Number 24970AZ-2505-2020
July 15, 2020FDAPercepta CRT-P MRI, Model Numbers: a) W1TR01, b) W1TR04, c) W4TR01, d) W4TR04Z-2511-2020
March 25, 2020FDAMedtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatr…Z-1524-2020
November 6, 2019FDAProgrammers & Remote Monitoring Software Apps: 29901 CareLink Encore ProgrammerZ-0240-2020
September 18, 2019FDAMedtronic Micra MC1VR01, REF MC1VR01 (OUS only). Cardiac pacemaker.Z-2493-2019
April 3, 2019FDAMedtronic Pulmonary Vein Ablation Catheter(R) GOLD (PVAC GOLD) 990078 - Product Usage: Th…Z-1069-2019
February 27, 2019FDAMedtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 ProgrammerZ-0845-2019
February 20, 2019FDAMedtronic implantable pulse generator: RELIA, Dual chamber pacemaker (VDD): (a) Model …Z-0808-2019
July 18, 2018FDAPercepta CRT-P MRI SureScan, REF W1TR01 Product Usage: The CRT-P models are implantab…Z-2412-2018
July 18, 2018FDAPercepta Quad CRT-P MRI SureScan, REF W4TR04 Product Usage: The CRT-P models are impl…Z-2415-2018

Questions about this company

How many recalls does Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) have?
Recalert has 25 U.S. recalls on record for Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), published between July 18, 2018 and June 28, 2023.
What was the most recent Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recall?
FDA recall Z-1744-2023, published June 28, 2023: CRT-D DTBB1QQ VIVA QUAD S IS4/DF4 US, Model Number DTBB1QQ; Implantable Cardioverter Defibrillators
Which agencies have handled Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls?
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) appears as the recalling firm in recalls from: FDA (25).

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