Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K172220 |
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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| Terumo Advanced Perfusion Assembly Pump Guts, 4 Inch, Catalog Number 801805 - Product Usage: is indi... | 2 | 02/07/2020 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo 220/240V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass proce... | 2 | 09/25/2018 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo 100/120V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass proce... | 2 | 09/25/2018 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Flowmeter Module (accessory to Terumo Advanced Perfusion System 1). Provides the interface betwe... | 2 | 04/20/2018 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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