Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K160457 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
FilmArray BCID Panel, RFIT-ASY-0126, 30, Rx Only, CE, IVD, UDI: 00815381020086 used with the follo... | 2 | 06/08/2020 | BioFire Diagnostics, LLC |
FilmArray BCID Panel, RFIT-ASY-0127, 6, Rx Only, CE, IVD, UDI: 00815381020093 used with the follow... | 2 | 06/08/2020 | BioFire Diagnostics, LLC |
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, wh... | 2 | 04/12/2019 | BioFire Diagnostics, LLC |
FilmArray Blood Culture Identification (BCID), IVD, Rx Only, BioFire Diagnostics, LLC, Panel Catalo... | 2 | 10/30/2018 | BioFire Diagnostics, LLC |
FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test ki... | 2 | 04/25/2018 | BioFire Diagnostics, LLC |
-