Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K123197 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
VERIGENE Clostridium difficile Nucleic Acid Test, REF 30-002-022 | 2 | 06/28/2023 | Luminex Corporation |
Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number: 20-006-022 | 2 | 07/02/2021 | Luminex Corporation |
The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative, multiplexed in vitro di... | 2 | 09/23/2014 | Nanosphere, Inc. |
Nanosphere Verigene Each CDF test consists of a Verigene CDF Nucleic Acid Test Kit and a Verigen... | 3 | 08/08/2014 | Nanosphere, Inc. |
-