Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K083842 |
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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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ROTROL P Control for ROTEM delta Thromboelastometry System, For In Vitro Diagnostic Use Only. Quali... | 2 | 03/09/2016 | TEM Systems Inc |
ROTROL P Control for ROTEM delta Thromboelastometry System, Manufactured for: Tem Innovations GmbH. | 2 | 04/03/2015 | TEM Systems Inc |
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