Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K140083 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023 | 2 | 06/28/2023 | Luminex Corporation |
Verigene EP Amplification Reagent Kit Test | 2 | 09/10/2021 | Luminex Corporation |
Verigene Enteric Pathogens Nucleic Acid Test (EP) Model Number: 20-006-023 | 2 | 07/02/2021 | Luminex Corporation |
VERIGENE Processor SP - Product Usage: intended for processing and identifying nucleic acids utilizi... | 2 | 04/23/2021 | Luminex Corporation |
The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed, qualitative test for simulta... | 2 | 09/23/2014 | Nanosphere, Inc. |
-