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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-1076-05 - Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopic imaging. Labeling is as follows: Product Label ''***Argon Medical Device***10cc Control Syring... 2 08/03/2005 FEI # 1625425
Argon Medical Devices, Inc
Z-1077-05 - Labeling is as follows: Product Labeling: ''***Argon Medical Devices***CUSTOM MANIFOLD KIT***REF/REORDER NO. 194902A***CONTENTS: 1 3-Port Manifold, 500 PSI***1 ASY CDX3 Transducer***1 Stopcock A... 2 08/03/2005 FEI # 1625425
Argon Medical Devices, Inc
Z-1081-05 - Labeling is as follows: Product labeling: ''***Argon Medical Devices***RE-ORDER NO./REF 193248***12cc Control Syringe***ST/FR/TR/FM w/ Reservoir***This device is designed for the administraion a... 2 08/03/2005 FEI # 1625425
Argon Medical Devices, Inc
Z-1079-05 - Labeling is as follows: Product Labeling: ''***Argon Medical Devices***MANIFOLD KIT***SINGLE USE ONLY***REF/REORDER NO. 094337***EtO STERILIZATION RECOMMENDED***Caution: For manufacturing, proc... 2 08/03/2005 FEI # 1625425
Argon Medical Devices, Inc
Z-1080-05 - Labeling is as follows: Product Labeling: ''***Argon Medical Devices***12cc Control Syringe***FR/TR/RM w/ Reservoir***SINGLE USE ONLY***REF/REORDER NO. 093209***This device is designed for the a... 2 08/03/2005 FEI # 1625425
Argon Medical Devices, Inc
Z-1078-05 - Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopic imaging. Labeling is as follows: Product Label ''***Argon Medical Device***REORDER NO./REF 193... 2 08/03/2005 FEI # 1625425
Argon Medical Devices, Inc
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