| Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-A recall (Z-0887-2008) | Argon Medical Devices, Inc | 2008-01-31 |
| Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-A recall (Z-0888-2008) | Argon Medical Devices, Inc | 2008-01-31 |
| Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-A recall (Z-0889-2008) | Argon Medical Devices, Inc | 2008-01-31 |
| Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-A recall (Z-0890-2008) | Argon Medical Devices, Inc | 2008-01-31 |
| Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-A recall (Z-0891-2008) | Argon Medical Devices, Inc | 2008-01-31 |
| Product consists of a syringe used to inject fluids during an angiographic procedure for f recall (Z-1076-05) | Argon Medical Devices, Inc | 2005-08-03 |
| Labeling is as follows: Product Labeling: ''***Argon Medical Devices***CUSTOM MANIFOLD KIT recall (Z-1077-05) | Argon Medical Devices, Inc | 2005-08-03 |
| Product consists of a syringe used to inject fluids during an angiographic procedure for f recall (Z-1078-05) | Argon Medical Devices, Inc | 2005-08-03 |
| Labeling is as follows: Product Labeling: ''***Argon Medical Devices***MANIFOLD KIT***SING recall (Z-1079-05) | Argon Medical Devices, Inc | 2005-08-03 |
| Labeling is as follows: Product Labeling: ''***Argon Medical Devices***12cc Control Syring recall (Z-1080-05) | Argon Medical Devices, Inc | 2005-08-03 |
| Labeling is as follows: Product labeling: ''***Argon Medical Devices***RE-ORDER NO./REF 19 recall (Z-1081-05) | Argon Medical Devices, Inc | 2005-08-03 |
| Argon Medical Devices, Vesseloops, Blue Maxi, Two Latex free silicone vessel ties. Quantit recall (Z-1044-04) | Argon Medical Devices, Inc | 2004-07-20 |