Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K051748 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397310, 14.5F, st... | 2 | 08/26/2019 | Bard Peripheral Vascular Inc |
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397350, 14.5F, st... | 2 | 08/26/2019 | Bard Peripheral Vascular Inc |
GlidePath Long-Term Hemodialysis Catheter, REF/Product code:5396280, 14.5F, Alphacurve, 28cm length,... | 2 | 08/26/2019 | Bard Peripheral Vascular Inc |
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