Ab Sciex recalls

7 recalls on record · latest: October 4, 2021

Official U.S. recall history for Ab Sciex, compiled from official government records.

Get recall alerts

Free email alert whenever Ab Sciex has a new recall — straight from official government data. Unsubscribe anytime.

AB SCIEX recalls Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid ch…

October 4, 2021 · Medical device recalls Moderate risk The values of the Internal Standard (IS) concentrations are incorrectly derived…

Ab Sciex recalls AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 5024501 3200MD series and 4500M…

June 16, 2016 · Medical device recalls Moderate risk MultiQuant MD software where under certain conditions a user can be presented w…

Ab Sciex recalls AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (REF): 503…

June 16, 2016 · Medical device recalls Moderate risk MultiQuant MD software where under certain conditions a user can be presented w…

Ab Sciex recalls AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (REF): 502…

June 16, 2016 · Medical device recalls Moderate risk MultiQuant MD software where under certain conditions a user can be presented w…

Ab Sciex recalls AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (REF…

June 16, 2016 · Medical device recalls Moderate risk MultiQuant MD software where under certain conditions a user can be presented w…

Ab Sciex recalls AB Sciex Triple Quad 4500MD LC/MS/MS System, Part No. 5031257; and QTRAP 4500MD LC/MS/MS System, Part No. 5031231. Mass…

March 25, 2016 · Medical device recalls Moderate risk Under certain conditions, mass spectrometers may report incorrect quantitative…

Ab Sciex recalls Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/MS System, Instrume…

February 24, 2016 · Medical device recalls Moderate risk Wrong quantitative results may be displayed in a report from the device, which…