Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062372 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S, LK018.10S Freelite aids... | 2 | 01/19/2017 | The Binding Site Group, Ltd. |
Human Lambda Free SPAPlus Kit Product Code: LK018.S Freelite aids in the detection and monitor... | 2 | 01/19/2017 | The Binding Site Group, Ltd. |
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