Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Z-0285-2019 - Magellan LeadCare® II Blood Lead Test Kit. In Vitro Test for the measurement of lead in fresh whole blood. Catalog Number: 70-6762 Primary DI No: 00850355006000 The LeadCare II Blood Lead Test ... | 2 | 10/26/2018 | Magellan Diagnostics, Inc. |
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