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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0209-2019 - APTIO INPUT/OUTPUT MODULE 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0210-2019 - APTIO RACK INPUT MODULE 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0211-2019 - APTIO CENTRIFUGE MODULE 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0212-2019 - APTIO 15000 REFRIGERATED STORAGE MODULE 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0217-2019 - STREAMLAB - REFRIGERATED STORAGE MODULE 15000 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0214-2019 - APTIO RACK OUTPUT MODULE 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0215-2019 - STREAMLAB CORE UNIT / LYNX WITH IOM 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0216-2019 - STREAMLAB - REFRIGERATED STORAGE MODULE 9000 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
Z-0213-2019 - APTIO 9000 REFRIGERATED STORAGE MODULE 2 10/23/2018 Siemens Healthcare Diagnostics, Inc.
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