Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K080807 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodia... | 2 | 09/19/2024 |
FEI # 2521402 B Braun Medical Inc |
| STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodia... | 2 | 09/19/2024 |
FEI # 2521402 B Braun Medical Inc |
| SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodi... | 2 | 09/19/2024 |
FEI # 2521402 B Braun Medical Inc |
| STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to transfer blood between a patient and a h... | 2 | 09/19/2024 |
FEI # 2521402 B Braun Medical Inc |
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