Medical Device Recalls
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1 result found
Recall Number: Z-0214-2022 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only This product s intende... | 2 | 11/10/2021 |
FEI # 3002564473 BioCheck, Inc. |
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