Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081767 |
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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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AmniSure ROM Test, Material Nos. FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Dist... | 2 | 04/01/2020 | Qiagen Sciences LLC |
AmniSure ROM Test under the following labels: 1) Catalog Number FMRT-1-25 and 2) Catalog Number FMRT... | 1 | 07/13/2018 | Qiagen Sciences, Inc. |
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