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Abbott Laboratories Inc. (St Jude Medical) Recalls
5 recalls on record · June 5, 2019 to June 23, 2021 · Medical Devices
Recalls by year
19
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 23, 2021Medical DevicesFDA
Abbott Laboratories Inc. (St Jude Medical) recalls WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012
Hazard: Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
June 23, 2021Medical DevicesFDA
Abbott Laboratories Inc. (St Jude Medical) recalls v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System Display, Model H700124, The WorkMate Claris"
Hazard: Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
June 23, 2021Medical DevicesFDA
Abbott Laboratories Inc. (St Jude Medical) recalls v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System, Model H700123. The WorkMate Claris" System is a
Hazard: Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
May 19, 2021Medical DevicesFDA
Abbott Laboratories Inc. (St Jude Medical) recalls NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000
Hazard: Potential capacitor failure which typically manifests as in inability to provide output on one or more channels. In some instances, users reported a charring/smoky odor or emission.
June 5, 2019Medical DevicesFDA
Abbott Laboratories Inc. (St Jude Medical) recalls TactiSys Quartz Equipment (with software version 1.7) Model: PN-004 400 Part Numbers: 600043767 (China), 100154367 (
Hazard: In reported cases, the device log on the TactiSys Quartz Equipment operating on Software Version 1.7.0 fills the allocated disk space, which prevents the storage of new log data. This may lead to intermittent contact force data to be displayed during the procedure.