Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K903505 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BacT/ALERT Classic System Software, Blood Culturing System | 2 | 05/03/2007 | bioMerieux, Inc. |
BacT/VIEW C.30a Software update (P/N 514515-1) diagnostic data management system, bioMerieux, Inc., ... | 2 | 03/22/2007 | bioMerieux, Inc. |
Bac T/ALERT® 3D 60 | 2 | 09/07/2005 | BIOMERIEUX, INC. |
Bac T/ALERT® 3D Control Module | 2 | 09/07/2005 | BIOMERIEUX, INC. |
Bac T/ALERT® 3D Combination Module | 2 | 09/07/2005 | BIOMERIEUX, INC. |
BacT/ALERT®(BTA) Classic instruments. | 3 | 02/01/2005 | bioMerieux |
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