Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K072549 |
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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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1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs, Ref: 7496000, UDI:(01)00801741027... | 2 | 03/26/2020 | Bard Peripheral Vascular Inc |
PowerPort isp M.R.I Implanted Port without Suture Plugs with attachable 6F Chronoflex Polyurethane O... | 2 | 04/29/2010 | Bard Access Systems |
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