Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K981522 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN VITRO DIAGNOSTIC USE ONLY... | 2 | 03/08/2021 | Tosoh Bioscience Inc |
Tosoh Bioscience AIA Analyte Application Manual (AAM) CD Part Number: 997027 CD contains analyte... | 3 | 08/15/2018 | Tosoh Bioscience Inc |
AIA-PACK TgAb CONTROL SET | 3 | 05/15/2017 | Tosoh Bioscience, Inc. |
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