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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 14 of 14 Results
510(K) Number: K010050
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Product Description
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FDA Recall
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ADVIA Centaur Folate (500 tests), REF SMN 10331250, Cat No. 00203473 In vitro diagnostic use in t... 2 09/10/2013 Siemens Healthcare Diagnostics, Inc
ADVIA Centaur Folate (500 Tests) SMN 10325366, Cat No. 06891541 In vitro diagnostic use in the qu... 2 09/10/2013 Siemens Healthcare Diagnostics, Inc
ADVIA Centaur Folate (100 Tests), SMN 10310308, Cat No. 06367974 In vitro diagnostic use in the ... 2 09/10/2013 Siemens Healthcare Diagnostics, Inc
Siemens Healthcare ADVIA Centaur Folate (FOL) 500 Test 06891541 100 Test 063... 2 12/11/2012 Siemens Healthcare Diagnostics, Inc
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