Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K991432 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Total Thyroxine (T4) ELISA; REF EIA-1781 | 2 | 11/29/2021 |
FEI # 2245285 DRG International, Inc. |
| 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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