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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
510(K) Number: K014241
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Product Description
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Recall
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FDA Recall
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Alsius Cool Line Catheter, Model CL-2295A 2 02/15/2007 Alsius Corporation
Alsius Cool Line Catheter, Model CL-2295AE 2 02/15/2007 Alsius Corporation
Alsius CoolGard Temperature Regulation System 3 01/10/2006 Alsius Corporation
Alsius CoolGard 3000 Temperature Regulation System 3 08/24/2005 Alsius Corporation
Alsius CoolGard 3000 patient temperature regulation system 2 11/25/2004 Alsius Corporation
Alsius CoolGuard 3000 Temperature Regulation System, Model CoolGuard 3000 2 07/23/2004 Alsius Corporation
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