Medical Device Recalls
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71 to 80 of 80 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-1407-2014 - K2 (synthetic Marijuana) Test Strip; LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1408-2014 - K2 (synthetic Marijuana) Test card; LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1409-2014 - Troponin I test Card (serum); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1410-2014 - Troponin I test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1411-2014 - Cardiac Panel Test (Serum); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1412-2014 - Cardiac Panel Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1413-2014 - Myoglobin Test Card (Serum); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1414-2014 - Myoglobin Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1415-2014 - CK-MB Test Card (serum); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
| Z-1416-2014 - CK-MB Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054 | 2 | 04/07/2014 |
FEI # 3005984081 LumiQuick Diagnostics Inc. |
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