Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K010050 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 (2500 tests), REF SMN 10340209, Cat No. 09132781 In vitro diagnostic use in ... | 2 | 09/10/2013 | Siemens Healthcare Diagnostics, Inc |
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 |
Siemens Healthcare ADVIA Centaur Folate (FOL) 500 Test 06891541 100 Test 063... | 2 | 12/11/2012 | Siemens Healthcare Diagnostics, Inc |
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