Medical Device Recalls
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171 to 180 of 500 Results
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Recall Date to: 09/12/2015 Firm: Philips Medical Systems |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Allura XPER FD20 | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Integris Allura Flat Detector 9C | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
MultiDiagnost Eleva | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Integris XPER FD10 F/C | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Allura XPER FD20/10 | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Allura XPER 10/10 | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Integris H5000F | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
Integris BH5000 | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
EasyDiagnost Eleva x-ray systems | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
OminDiagnost Eleva | 2 | 09/24/2009 | Philips Medical Systems North America Co. Phillips |
* The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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