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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Related Medical Device Recalls Date Classified to: 04/25/2014
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Product Description
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Recall
Class
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Date
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Recalling Firm
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Z-2952-2011 - Spectranetics Turbo-Booster Laser Guide Catheter, 8 Fr, REF 518-063, Sterile EO, Spectranetics Corporation, 96 Talamine Court, Colorado Springs, CO 80907. Designed for directing and supporting Spec... 2 Aug-04-2011 Spectranetics Corporation
Z-2951-2011 - Spectranetics Turbo-Booster Laser Guide Catheter, 7 Fr, REF 518-043, Sterile EO, Spectranetics Corporation, 96 Talamine Court, Colorado Springs, CO 80907. Designed for directing and supporting Spec... 2 Aug-04-2011 Spectranetics Corporation
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