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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Reinforced Dual Lumen Cannula, 16Fr., REF: VV16F, Sterile EO Indications: The OriGen Reinforced D... | 2 | 10/18/2018 | OriGen Biomedical, Inc. |
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula... | 2 | 10/18/2018 | OriGen Biomedical, Inc. |
Reinforced Dual Lumen Cannula, 32Fr., REF: VV32F, Sterile EO Indications: The OriGen Reinforced ... | 2 | 10/18/2018 | OriGen Biomedical, Inc. |
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula... | 2 | 10/12/2018 | OriGen Biomedical, Inc. |
The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement ... | 1 | 10/20/2017 | OriGen Biomedical, Inc. |
OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE: DO NOT RE-USE Manufacture... | 1 | 04/23/2015 | OriGen Biomedical, Inc. |
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