Medical Device Recalls
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11 to 13 of 13 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1801-2024 - Medtronic Cardioplegia Adapters: a) DLP® 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number 25009, b) DLP® 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter, Model Number... | 2 | 05/10/2024 | Medtronic Perfusion Systems |
Z-1793-2024 - Medtronic Arterial Cannulae packaged as: a) DLP® Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020; b) DLP® Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220; c) DLP® Curv... | 2 | 05/10/2024 | Medtronic Perfusion Systems |
Z-1800-2024 - Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP® 9 Ga (11 Fr) Aortic Root Cannula, Model Number 24009; b) DLP® 16 Ga (5 Fr) Cardioplegia Needle Neonatal 0.64 cm (1/4 in) Tip Le... | 2 | 05/10/2024 | Medtronic Perfusion Systems |
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