Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110904 |
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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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Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use, in the quality control of... | 2 | 08/23/2023 | Randox Laboratories Ltd. |
Liquid Urine Control Level 3 For Professional Use in the quality control monitoring of In-Vitro D... | 3 | 05/26/2017 | Randox Laboratories |
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