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U.S. Department of Health and Human Services

Medical Device Recalls
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Product Description
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FDA Recall
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Philips MX8000 Dual v. EXP CT Scanner, utilizing V2.0 software. 3 05/15/2003 FEI # 1525965
Philips Medical Systems (Cleveland) Inc
MaxForce TTS High Performance Esophageal Balloon Dilatation Catheter 18mm/54 Fr 2 05/15/2003 FEI # 3001451463
Boston Scientific Corporation
MaxForce TTS High Performance Esophageal Balloon Dilatation Catheter 8mm/24 Fr 2 05/15/2003 FEI # 3001451463
Boston Scientific Corporation
MaxForce TTS High Performance Esophageal Balloon Dilatation Catheter 14mm/42 Fr 2 05/15/2003 FEI # 3001451463
Boston Scientific Corporation
MaxForce TTS High Performance Esophageal Balloon Dilatation Catheter 15mm/45 Fr 2 05/15/2003 FEI # 3001451463
Boston Scientific Corporation
Dr. Fog Endoscopic Fog Prevention Kit; model DF-3120. Each box contains 40 packages. Each package ... 2 05/15/2003 FEI # 3002750084
Aspen Surgical Products, Inc.
BD First PICC 3F 65 cm Single Lumen Procedure Kit. 3 05/15/2003 FEI # 1710034
Becton Dickinson Infusion Therapy
Permobil Chairman 2K powered wheelchair 2 05/15/2003 FEI # 1221084
Permobile Inc.
Somatom Sensation 16, Computed Tomography System, Diagnostic Imaging. 2 05/16/2003 FEI # 2240869
Siemens Medical Solutions USA, Inc
Leonardo MM-WS systems. System, Image Processing. 2 05/16/2003 FEI # 2240869
Siemens Medical Solutions USA, Inc

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