Medical Device Recalls
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1 to 7 of 7 Results
PMA Number: P810046 |
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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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Voyager RX Coronary Dilatation Catheter | 2 | 04/13/2005 | Guidant Corporation Advanced CardiovascularSystem |
VOYAGER NC Coronary Dilatation Catheter, 4.5 X 12.0 mm. The device is used for in the following: ... | 2 | 02/03/2009 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
VOYAGER NC Coronary Dilatation Catheter, 4.5 X 8.0 mm. The device is used for in the following: ... | 2 | 02/03/2009 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
POWERSAIL Coronary Dilatation Catheter: 2.75x18mm (US) Part #1005522-18 | 1 | 07/29/2009 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
POWERSAIL Coronary Dilatation Catheter: 4.0x8mm (CE) Part #1005726-08 | 1 | 07/29/2009 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
POWERSAIL Coronary Dilatation Catheter: 3.25x8mm (US) Part #1005524-08 | 1 | 07/29/2009 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
POWERSAIL Coronary Dilatation Catheter: 3.25x18mm (US) Part #1005524-18 | 1 | 07/29/2009 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
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