Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K964052 |
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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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HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture Catalogue number: 171.002.... | 2 | 11/28/2018 | EUROTROL INC |
HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture. Catalogue number: 171.003... | 2 | 11/28/2018 | EUROTROL INC |
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