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U.S. Department of Health and Human Services

Medical Device Recalls
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Recall Date to: 03/06/2015 PMA Number: P050018
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Product Description
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FDA Recall
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AngioSculpt Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter, cutting/scoring, Easy Ex... 1 08/18/2010 AngioScore Inc.
AngioSculpt PTCA Scoring Balloon Catheter, Catalog (REF) Number: 2027-2510, size 2.5mm x 10 mm, Angi... 3 01/23/2008 AngioScore Inc.
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