Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K113869 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F | 1 | 06/04/2019 | OriGen Biomedical, Inc. |
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV23F | 1 | 06/04/2019 | OriGen Biomedical, Inc. |
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV32F | 1 | 06/04/2019 | OriGen Biomedical, Inc. |
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV13F | 1 | 06/04/2019 | OriGen Biomedical, Inc. |
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV19F | 1 | 06/04/2019 | OriGen Biomedical, Inc. |
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV28F | 1 | 06/04/2019 | OriGen Biomedical, Inc. |
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