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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0320-2017 - IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay, REF/Catalog Number L2KCM2(D) - 200 tests (US), SMN 10370302 (US), UDI 00630414985725 (US); and REF/Catalog Number L2KCM2 - 200 tests (OUS), S... 2 10/27/2016 Siemens Healthcare Diagnostics, Inc.
Z-0319-2017 - IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Siemens Material Number (SMN) 10370301 (US), Unique Device Identification Number (UDI) 00630414985718 (... 2 10/27/2016 Siemens Healthcare Diagnostics, Inc.
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