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U.S. Department of Health and Human Services

Medical Device Recalls

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121 to 130 of 500 Results *
Recall Date to: 04%2F08%2F2014
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Product Description
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Recall
Class
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FDA Recall
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AB SCIEX 3200MD QTRAP® LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instrument ... 2 08/12/2016 Ab Sciex
AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 5024501 32... 2 08/12/2016 Ab Sciex
AB Sciex Triple Quad 4500MD LC/MS/MS System, Part No. 5031257; and QTRAP 4500MD LC/MS/MS System, Par... 2 05/15/2016 Ab Sciex
Analyst® MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/... 2 04/29/2016 Ab Sciex
AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identi... 2 09/08/2014 Ab Sciex
Citrine Triple Quad Mass Spectrometer, Part Number 5063684 2 10/05/2023 AB Sciex, LLC
API3200MD Mass Spectrometer, Part Number 4466230 2 10/05/2023 AB Sciex, LLC
Citrine QTRAP Mass Spectrometer, Part Number 5063685 2 10/05/2023 AB Sciex, LLC
4500MD Triple Quad Mass Spectrometer, Part Number 5032522 2 10/05/2023 AB Sciex, LLC
1500 Flex Heat and Moisture Exchanger, Catalog Reference 150 - Product Usage: Heat Moisture Exchang... 2 10/06/2020 AB ULAX

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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