Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K030099 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Ultra-Filtration (UF) Removal Regulators(Rgltr Assy UF REM Molded Spare); a spare part used with Bax... | 3 | 07/25/2006 | Baxter Healthcare Renal Div |
System 1000 family of Hemodialysis Instruments, including the System 1000, TINA, AURORA and ARENA; B... | 2 | 01/06/2006 | Baxter Healthcare Renal Div |
Baxter Arena Hemodialysis Systems, product codes ARENADPX, ARENASP, ARENADPP, ARENASPX; Baxter Healt... | 2 | 08/24/2005 | Baxter Healthcare Renal Div |
System 1000 family of Hemodialysis Instruments, including the System 1000, Arena, 1550, BM11, BM25 a... | 2 | 12/24/2004 | Baxter Healthcare Renal Div |
Baxter Arena Hemodialysis Delivery System; Baxter Healthcare Corporation, Renal Division, McGaw Park... | 2 | 07/20/2004 | Baxter Healthcare Renal Div |
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