Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K042910 |
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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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Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. ... | 1 | 05/22/2017 | Vascular Solutions, Inc. |
Vascular Solutions Venture Rx Catheter, 6F, resterilized. | 2 | 09/13/2018 | SPS Sterilization, Inc |
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