Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K193379 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP | 2 | 10/28/2022 | Edwards Lifesciences, LLC |
| Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 12080... | 2 | 10/28/2022 | Edwards Lifesciences, LLC |
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