Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K981624 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 ... | 2 | 04/12/2024 | Baxter Healthcare Corporation |
| Baxter Flo-Thru Intraluminal Shunt, Product Codes: a) Product Code FT12100, 1.00 GLOBAL; b) Prod... | 2 | 01/05/2024 | Baxter Healthcare Corporation |
| Flo-Thru Intraluminal Shunt. Used in coronary artery or peripheral vascular procedures. Used to shun... | 2 | 04/29/2022 | Baxter Healthcare Corporation |
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