Medical Device Recalls
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1 to 10 of 40 Results
510(K) Number: K033737 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AD6 table, modified, used with the XPER systems. The modification on the table is the cables used ... | 2 | 11/29/2005 | Philips Medical Systems North America Co. Phillips |
AD5 table, modified, used with the XPER x-ray systems. The modification on the table is the cables... | 2 | 11/29/2005 | Philips Medical Systems North America Co. Phillips |
Allura Xper FD10 x-ray system | 2 | 02/28/2006 | Philips Medical Systems North America Co. Phillips |
Allura Xper FD 20/10 x-ray, and fluoroscopy | 2 | 11/14/2006 | Philips Medical Systems North America Co. Phillips |
Allura Xper FD20 X-Ray System, Release 2.2, Philips Medical Systems, Bothell, WA 98021 | 2 | 12/07/2007 | Philips Medical Systems North America Co. Phillips |
Allura Xper FD20/10, Release 1.2, Philips Medical Systems, Bothell, WA 98021 | 2 | 12/07/2007 | Philips Medical Systems North America Co. Phillips |
Allura XPER FD20/10 | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Allura XPER FD20 | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Philips Allura XPER FD20 Angiographic X-ray system. This system with Velara Generator can be identi... | 2 | 09/22/2010 | Philips Medical Systems North America Co. Phillips |
Philips Allura XPER FD 20/10 Angiographic X-ray system. This system with Velara Generator can be id... | 2 | 09/22/2010 | Philips Medical Systems North America Co. Phillips |
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