Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K142705 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number: 80-0010 | 1 | 05/18/2017 |
FEI # 1218996 Magellan Diagnostics, Inc. |
| LeadCare Plus Blood Lead Analyzer Part Number: 82-0001 Intended for the quantitative measurement... | 2 | 04/03/2018 |
FEI # 1218996 Magellan Diagnostics, Inc. |
| LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 | 1 | 07/01/2021 |
FEI # 1218996 Magellan Diagnostics, Inc. |
| LeadCare® Plus Blood Lead Test Kit; Catalog Number: 82-0004; The LeadCare® Plus kit is provided wi... | 2 | 04/17/2026 |
FEI # 1218996 Magellan Diagnostics, Inc. |
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