Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K050374 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11532401. in vitro diagnostic assay | 2 | 10/20/2022 | Siemens Healthcare Diagnostics, Inc. |
| Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay | 2 | 10/20/2022 | Siemens Healthcare Diagnostics, Inc. |
| Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637 | 2 | 04/14/2022 | Siemens Healthcare Diagnostics, Inc. |
| ADVIA Chemistry Calibrator | 2 | 06/26/2020 | Siemens Healthcare Diagnostics, Inc. |
| Advia Chemistry Calibrator For in vitro diagnostic use in the calibration of ADVIA® Chemistry syst... | 2 | 11/16/2016 | Siemens Healthcare Diagnostics, Inc. |
| Siemens Chemistry Calibrator (CAL) used with the ADVIA Chemistry Direct Bilirubin_2 Reagent, Siemens... | 2 | 11/19/2013 | Siemens Healthcare Diagnostics |
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