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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K072676
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FDA Recall
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Siemens ACUSON X300 Systems with software versions 3.0.00 and 3.0.02, model numbers 10348531, 103485... 2 05/06/2011 Siemens Medical Solutions USA, Inc.
Acuson X300 systems at software versions 1.00.00 to 1.0.10 and 2.0.00 to 2.0.02, model numbers 10037... 2 04/25/2011 Siemens Medical Solutions USA, Inc.
Siemens ACUSON X300 Premium Edition Systems with software versions 5.0.00 and 5.0.01 (model numbers ... 2 04/25/2011 Siemens Medical Solutions USA, Inc.
ACUSON X300, X300 PE and SONOVISTA X300 (all versions) with cardiovascular options installed; ACUSO... 2 03/28/2011 Siemens Medical Solutions USA, Inc., Mountain View, CA
Siemens Ultrasound, Acuson/Sonovista X300 ultrasound systems, software revisions 2.0.1 to 2.0.05, 3.... 2 10/10/2008 Siemens Medical Solutions USA, Inc.
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