Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K040579 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The Alere Cholestech LDX® high sensitivity C-Reactive Protein (hsCRP) Test Cassette, Model Number 12... | 2 | 04/25/2013 | Alere San Diego, Inc. |
| Cholestech LDX High Sensitivity C-Reactive Protein (hs-CRP) Test Cassette. The Cholestech LDX high ... | 3 | 09/20/2008 | Cholestech Corp |
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