Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K972608 |
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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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Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use, in the quality control of... | 2 | 01/05/2023 | Randox Laboratories Ltd. |
Liquid Assayed Specific Protein- In vitro diagnostic use, in the quality control of serum on clinica... | 2 | 01/05/2023 | Randox Laboratories Ltd. |
Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use, in the quality control of ... | 2 | 01/05/2023 | Randox Laboratories Ltd. |
Randox Liquid Assayed Specific Protein Control - Level 2 (SP Control 2), Cat. no. PS2683 | 2 | 06/13/2018 | Randox Laboratories Ltd. |
Randox Liquid Assayed Specific Protein Control - Level 1 (SP Control 1), Cat. no. PS2682 | 2 | 06/13/2018 | Randox Laboratories Ltd. |
Randox Liquid Assayed Specific Protein Control - Level 3 (SP Control 3), Cat. no. PS2684 | 2 | 06/13/2018 | Randox Laboratories Ltd. |
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