Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K130896 |
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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 Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM, 1.... | 2 | 01/05/2024 | Baxter Healthcare Corporation |
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