Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120988 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 | 2 | 09/12/2024 | Medtronic Perfusion Systems |
| Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedure... | 2 | 03/05/2013 | Medtronic Inc. Cardiac Rhythm Disease Management |
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