Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K072657 |
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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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PORT-A-CATH® II POWER P.A.C. Low Profile" system. | 2 | 07/04/2020 | Smiths Medical ASD Inc. |
GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN SYSTEM. Labeled as the following item d... | 2 | 10/24/2019 | Smiths Medical ASD Inc. |
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