Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K122584 |
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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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Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400 | 2 | 03/03/2018 | Instrumentation Laboratory Co. |
Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 - Product Usage - HemosIL® ReadiPlasTin i... | 2 | 10/05/2018 | Instrumentation Laboratory Co. |
HemosIL ReadiPlasTin, Part No. 0020301400 | 2 | 05/10/2022 | Instrumentation Laboratory |
HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An in vitro diagnostic thromboplastin reagent... | 2 | 11/23/2021 | Instrumentation Laboratory |
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