Home / Recalls / Medical Devices
Philips North America recalls CombiDiagnost R90 R.1.0
Recalled May 24, 2023 · FDA recall Z-1588-2023 · Philips North America
Hazard
Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0, CombiDiagnost R90 R.1.0 and CombiDiagnost R90 R1.1 systems are missing a certification label required by the Food and Drug Administration (FDA). · FDA Class II
Units
25 systems in total
Sold at
US Nationwide
Description
Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0, CombiDiagnost R90 R.1.0 and CombiDiagnost R90 R1.1 systems are missing a certification label required by the Food and Drug Administration (FDA).
Product
CombiDiagnost R90 R.1.0
Manufacturer(s)
Philips North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →