Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K111725 |
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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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MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007 | 2 | 02/14/2024 | SEDECAL SA |
Mobile Diagnostic X-Ray System with Digital Panel | 2 | 04/04/2017 | Philips Healthcare Inc. |
Sedecal SA Mobile Diagnost w DR x-ray system | 2 | 06/03/2016 | Sedecal USA, Inc. |
Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doc... | 2 | 03/08/2016 | Sedecal S.A. |
MobileDiagnost wDR motorized portable diagnostic X-ray systems. | 2 | 02/02/2015 | Sedecal S.A. |
Intended for both adult and pediatric patients for taking diagnostic radiographic exposures of the s... | 2 | 12/16/2014 | Philips Medical Systems, Inc. |
Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography X-Ray System Product Usa... | 2 | 08/21/2013 | Philips Healthcare Inc. |
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