Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K234064 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Cathe... | 1 | 02/06/2026 | Medline Industries, LP |
| Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and intra-luminal visualization of ca... | 1 | 09/26/2025 | Medline Industries, LP |
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