Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K100364 |
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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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| Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis ... | 2 | 06/01/2020 | Baxter Healthcare Corporation |
| Gambro Cartridge Blood Transport System for Hemodialysis Blood Set - Product Usage: is intended for ... | 2 | 06/01/2020 | Baxter Healthcare Corporation |
| Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood Set - Product Usage: is in... | 2 | 06/01/2020 | Baxter Healthcare Corporation |
| Gambro Cartridge Low Weight-Low Volume Blood Transport System for Hemodialysis Blood Set - Product U... | 2 | 06/01/2020 | Baxter Healthcare Corporation |
| Gambro Cartridge Low Weight-Low Volume Blood Transport System for Hemodialysis Blood Set, product co... | 2 | 02/16/2021 | Baxter Healthcare Corporation |
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