Medical Device Recalls
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11 to 16 of 16 Results
PMA Number: P060040 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| HeartMate® II LVAS with Pocket Controller; 106762 - HMII POCKET CONTROLLER, NA; UDI: 008130240112... | 1 | 05/24/2017 | Thoratec Corporation |
| HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend ... | 1 | 03/22/2024 | Thoratec Corp. |
| Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L128... | 1 | 06/07/2024 | Thoratec Corp. |
| HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Re... | 1 | 04/17/2025 | Thoratec LLC |
| Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 ... | 1 | 08/13/2025 | Thoratec LLC |
| Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 Software Versi... | 1 | 08/13/2025 | Thoratec LLC |
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