Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K123563 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 | 1 | 07/01/2021 | Magellan Diagnostics, Inc. |
Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010 | 1 | 05/18/2017 | Magellan Diagnostics, Inc. |
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