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 System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK, Catalog Number 5785 - Pro... | 2 | 09/12/2020 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32, Catalog Number 5791 - Product Usa... | 2 | 09/12/2020 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32, Catalog Number 5773 - Product Usa... | 2 | 09/12/2020 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo® Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188 | 2 | 10/18/2018 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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