AB Sciex Recalls
12 recalls on record · September 17, 2014 to October 11, 2023 · Medical Devices
Recalls by year
14
16
21
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 11, 2023Medical DevicesFDA
AB Sciex, LLC recalls Citrine Triple Quad Mass Spectrometer, Part Number 5063684
Hazard: In rare occasions, the combination of a leak of a highly flammable solvent at the ion source probe, and an electrical discharge may result in a flame on top of the probe and possible ejection of the electrode assembly from the probe. There is a risk to the patient/user, customer property, or environment because there is a potential for a health risk and property damage should the flame be left unattended. The failure causes a delay in patient results.
October 11, 2023Medical DevicesFDA
AB Sciex, LLC recalls Citrine QTRAP Mass Spectrometer, Part Number 5063685
Hazard: In rare occasions, the combination of a leak of a highly flammable solvent at the ion source probe, and an electrical discharge may result in a flame on top of the probe and possible ejection of the electrode assembly from the probe. There is a risk to the patient/user, customer property, or environment because there is a potential for a health risk and property damage should the flame be left unattended. The failure causes a delay in patient results.
October 11, 2023Medical DevicesFDA
AB Sciex, LLC recalls 4500MD Triple Quad Mass Spectrometer, Part Number 5032522
Hazard: In rare occasions, the combination of a leak of a highly flammable solvent at the ion source probe, and an electrical discharge may result in a flame on top of the probe and possible ejection of the electrode assembly from the probe. There is a risk to the patient/user, customer property, or environment because there is a potential for a health risk and property damage should the flame be left unattended. The failure causes a delay in patient results.
October 11, 2023Medical DevicesFDA
AB Sciex, LLC recalls API3200MD Mass Spectrometer, Part Number 4466230
Hazard: In rare occasions, the combination of a leak of a highly flammable solvent at the ion source probe, and an electrical discharge may result in a flame on top of the probe and possible ejection of the electrode assembly from the probe. There is a risk to the patient/user, customer property, or environment because there is a potential for a health risk and property damage should the flame be left unattended. The failure causes a delay in patient results.
November 3, 2021Medical DevicesFDA
AB SCIEX recalls Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid chr
Hazard: The values of the Internal Standard (IS) concentrations are incorrectly derived when the user builds a customized test, then set the IS column to hidden and left the column empty. This may lead to the user making incorrect conclusions using incorrect results.
August 24, 2016Medical DevicesFDA
Ab Sciex recalls AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (REF): 5
Hazard: MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
August 24, 2016Medical DevicesFDA
Ab Sciex recalls AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (R
Hazard: MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
August 24, 2016Medical DevicesFDA
Ab Sciex recalls AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (REF): 5
Hazard: MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
August 24, 2016Medical DevicesFDA
Ab Sciex recalls AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 5024501 3200MD series and 4500
Hazard: MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
May 25, 2016Medical DevicesFDA
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. Ma
Hazard: Under certain conditions, mass spectrometers may report incorrect quantitative results.
May 11, 2016Medical DevicesFDA
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, Instrumen
Hazard: Wrong quantitative results may be displayed in a report from the device, which may potentially lead to an incorrect patient diagnosis.
September 17, 2014Medical DevicesFDA
Ab Sciex recalls AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or orga
Hazard: Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis