Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K032431 |
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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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Prisma M60 POSTDILUTION set. Product number 104183. Each set is packaged in a plastic pouch, 4 pouch... | 2 | 08/13/2014 | Gambro Renal Products, Incorporated |
Prisma M 60 PRE set (new design). Product number 103658. Each set is packaged in a plastic pouch, 4 ... | 2 | 08/13/2014 | Gambro Renal Products, Incorporated |
Prisma M100 PRE pump infusion set. Product number 107791. Each set is packaged in a plastic pouch, 4... | 2 | 08/13/2014 | Gambro Renal Products, Incorporated |
Prisma M 100 PRE set. Product number 103657. Each set is packaged in a plastic pouch, 4 pouches per ... | 2 | 08/13/2014 | Gambro Renal Products, Incorporated |
Prisma M100 set. Product number 104182. Each set is packaged in a plastic pouch, 4 pouches per carto... | 2 | 08/13/2014 | Gambro Renal Products, Incorporated |
Gambro Prisma M100 preset, Part No. 8353486. | 2 | 04/05/2006 | Gambro Renal Products, Inc. |
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