Abbott Laboratories Inc. (St Jude Medical) FDA Recalls

4 recalls on file across devices, 0 of them Class I and 0 still open. Matched by name to ABT.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012Class IIMay 5, 2021Due to a software error, the user may lose functionality of	Due to a software error, the user may lose functionality of the system or the screen may turn black during ope	Class IIDevices	May 5, 2021
v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System Display, Model H700124, The WorkMate Claris" Class IIMay 5, 2021Due to a software error, the user may lose functionality of	Due to a software error, the user may lose functionality of the system or the screen may turn black during ope	Class IIDevices	May 5, 2021
v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System, Model H700123. The WorkMate Claris" System is aClass IIMay 5, 2021Due to a software error, the user may lose functionality of	Due to a software error, the user may lose functionality of the system or the screen may turn black during ope	Class IIDevices	May 5, 2021
NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000Class IIApr 22, 2021Potential capacitor failure which typically manifests as in	Potential capacitor failure which typically manifests as in inability to provide output on one or more channel	Class IIDevices	Apr 22, 2021