Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K971640 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LeadCare Blood Lead Testing System Kits Catalog Number: 70-2233 | 2 | 06/21/2005 |
FEI # 1218996 Esa Biosciences, Inc. |
| Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage: The LeadCare Blood Lead... | 1 | 06/05/2017 |
FEI # 1218996 Magellan Diagnostics, Inc. |
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