Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls |
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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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| Z-2159-2018 - Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206, Article Number A20-0101. For use in cardiopulmonary bypass | 2 | 06/11/2018 |
FEI # 3009507273 Maquet Cardiopulmonary Ag |
| Z-2161-2018 - Aortic Arterial Cannula 24 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002267, Article Number A24-7107. For use in cardiopulmonary bypass | 2 | 06/11/2018 |
FEI # 3009507273 Maquet Cardiopulmonary Ag |
| Z-2160-2018 - Aortic Arterial Cannula 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002246, Article Number A22-7107. For use in cardiopulmonary bypass | 2 | 06/11/2018 |
FEI # 3009507273 Maquet Cardiopulmonary Ag |
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