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Device recall: Philips Azurion 3 M12. Model Numbers: 722063, 722221. (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)

U.S. FDA device recalls via openFDA0 comments

Open, Classified. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized…

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