Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K012774 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206... | 2 | 06/11/2018 | Maquet Cardiopulmonary Ag |
Aortic Arterial Cannula 24 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002... | 2 | 06/11/2018 | Maquet Cardiopulmonary Ag |
Aortic Arterial Cannula 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 70100... | 2 | 06/11/2018 | Maquet Cardiopulmonary Ag |
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