Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K182188 |
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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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Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Ster... | 2 | 10/15/2021 | Intuitive Surgical, Inc. |
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the... | 2 | 11/25/2020 | Intuitive Surgical, Inc. |
Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845. | 2 | 09/10/2020 | Intuitive Surgical, Inc. |
ION Reprocessing Accessories Kit, IF1000 (Part Number: 490024-03) UDI:00886874119129. The kit includ... | 2 | 09/10/2020 | Intuitive Surgical, Inc. |
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