Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K140522 |
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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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Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality control material to monitor ... | 3 | 06/28/2023 | Randox Laboratories Ltd. |
Immunoassay Premium Control Tri Level-In vitro diagnostic use, as assayed quality control material t... | 3 | 06/28/2023 | Randox Laboratories Ltd. |
Immunoassay Premium Plus Controls, Model Numbers IA3109 and IA3112 Product Usage: This product i... | 3 | 04/08/2019 | Randox Laboratories Ltd. |
Immunoassay Premium Controls (3x4x5mL and 12x5mL packages) | 3 | 03/12/2018 | Randox Laboratories |
Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages) | 3 | 03/12/2018 | Randox Laboratories |
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