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U.S. Department of Health and Human Services

Medical Device Recalls
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191 to 200 of 500 Results *
Recall Date to: 12/22/2014
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Product Description
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FDA Recall
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Bard Orbiter PV Steerable Catheter Item #: 320100 (Marketed in Europe Only) 2 02/28/2003 C. R.Bard, Inc./Electrophysiology Division
Bard Orbiter ST Artrial Mapping Steerable Catheter Item Numbers 320001 7FAM00001 7FAM00010 7FAM000... 2 02/28/2003 C. R.Bard, Inc./Electrophysiology Division
Bard Stinger SM Ablation Catheter Item Numbers 210001SM 218501SM 210002SM 218502SM 210003SM 21... 2 02/28/2003 C. R.Bard, Inc./Electrophysiology Division
Bard Stinger S Ablation Catheter: Item Numbers 210001S 218501S 6210015S 210002S 218502S 6210016... 2 02/28/2003 C. R.Bard, Inc./Electrophysiology Division
Bard Stinger M Ablation Catheters: Item Numbers 210001M 218501M 210002M 218502M 210003M 218503... 2 02/28/2003 C. R.Bard, Inc./Electrophysiology Division
Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 ... 2 02/28/2003 C. R.Bard, Inc./Electrophysiology Division
Viridia/Agilent Information Center Model : M3150A#C01 2 02/28/2003 Philips Medical Systems, Inc. Cardiac & Monitoring Systems
Intellivue Information Center Model: M3150B#C01 2 02/28/2003 Philips Medical Systems, Inc. Cardiac & Monitoring Systems
Intellivue Information Center Model: M3150BU#CO1 2 02/28/2003 Philips Medical Systems, Inc. Cardiac & Monitoring Systems
Viridia/Agilent Information Center Model : M3151A#CO1 2 02/28/2003 Philips Medical Systems, Inc. Cardiac & Monitoring Systems

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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