Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K053153 |
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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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Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based... | 2 | 05/03/2024 | Randox Laboratories Ltd. |
Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assay... | 2 | 01/18/2024 | Randox Laboratories Ltd. |
Calibration Serum Level 3 - IVD For use as a Calibrator in clinical chemistry assays Catalog Number... | 2 | 01/18/2024 | Randox Laboratories Ltd. |
Calibration Serum Level 3 CAL2351 | 2 | 01/18/2024 | Randox Laboratories Ltd. |
Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator. Catalogue Number: CAL2351 | 2 | 05/12/2021 | Randox Laboratories Ltd. |
This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry... | 3 | 09/07/2019 | Randox Laboratories Ltd. |
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